Linked Data
ClinVar Variation Id:
406860
dbSNP Id:
rs765792042
ExAC:
1:45798432 T / C
gnomAD v2:
1-45798432-T-C
gnomAD v3:
1-45332760-T-C
gnomAD v4:
1-45332760-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45332760T>C , CM000663.2:g.45332760T>C | GRCh38 |
| NC_000001.10:g.45798432T>C , CM000663.1:g.45798432T>C | GRCh37 |
| NC_000001.9:g.45571019T>C | NCBI36 |
| NG_008189.1:g.12711A>G , LRG_220:g.12711A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000412971.6:c.108+3A>G | ENSP00000410263.2:n.108+3A>G | |
| ENST00000435155.2:c.525+3A>G | ENSP00000403655.2:n.525+3A>G | |
| ENST00000467459.6:c.492+3A>G | ENSP00000435889.2:n.492+3A>G | |
| ENST00000483127.2:c.510+3A>G | ENSP00000436469.2:n.510+3A>G | |
| ENST00000485271.6:c.492+3A>G | ENSP00000431264.2:n.492+3A>G | |
| ENST00000529892.6:c.534+3A>G | ENSP00000432528.2:n.534+3A>G | |
| ENST00000533178.6:c.116-73A>G | ENSP00000436430.2:n.116-73A>G | |
| ENST00000672314.2:c.492+3A>G | ENSP00000500828.2:n.492+3A>G | |
| ENST00000674679.2:c.*404+3A>G | ENSP00000501623.2:n.*404+3A>G | |
| ENST00000710952.2:c.576+3A>G MANE Plus Clinical | ENSP00000518552.2:n.576+3A>G | |
| ENST00000672818.3:c.567+3A>G | ENSP00000500891.1:n.567+3A>G | |
| ENST00000450313.6:c.502+3A>G | ENSP00000408176.2:n.502+3A>G | |
| ENST00000456914.7:c.492+3A>G MANE Select | ENSP00000407590.2:n.492+3A>G | |
| ENST00000461495.6:c.*231+3A>G | ENSP00000437166.1:n.*231+3A>G | |
| ENST00000671856.1:n.438+3A>G | ||
| ENST00000671898.1:c.1080+3A>G | ENSP00000499896.1:n.1080+3A>G | |
| ENST00000672011.1:c.460+3A>G | ENSP00000500418.1:n.460+3A>G | |
| ENST00000672314.1:c.492+3A>G | ENSP00000500828.1:n.492+3A>G | |
| ENST00000672593.1:c.*308A>G | ENSP00000500455.1:n.*308A>G | |
| ENST00000672764.1:c.451+3A>G | ENSP00000500886.1:n.451+3A>G | |
| ENST00000672818.2:c.567+3A>G | ENSP00000500891.1:n.567+3A>G | |
| ENST00000673134.1:c.*189+3A>G | ENSP00000500526.1:n.*189+3A>G | |
| ENST00000674679.1:c.520+3A>G | ENSP00000501623.1:n.520+3A>G | |
| ENST00000354383.10:c.495+3A>G | ENSP00000346354.6:n.495+3A>G | |
| ENST00000355498.6:c.492+3A>G | ENSP00000347685.2:n.492+3A>G | |
| ENST00000372098.7:c.567+3A>G | ENSP00000361170.3:n.567+3A>G | |
| ENST00000372104.5:c.492+3A>G | ENSP00000361176.1:n.492+3A>G | |
| ENST00000372110.7:c.537+3A>G | ENSP00000361182.3:n.537+3A>G | |
| ENST00000372115.7:c.534+3A>G | ENSP00000361187.3:n.534+3A>G | |
| ENST00000412971.5:c.108+3A>G | ENSP00000410263.1:n.108+3A>G | |
| ENST00000435155.1:c.525+3A>G | ENSP00000403655.1:n.525+3A>G | |
| ENST00000448481.5:c.525+3A>G | ENSP00000409718.1:n.525+3A>G | |
| ENST00000450313.5:c.576+3A>G | ENSP00000408176.1:n.576+3A>G | |
| ENST00000456914.6:c.492+3A>G | ENSP00000407590.2:n.492+3A>G | |
| ENST00000461495.5:c.*231+3A>G | ENSP00000437166.1:n.*231+3A>G | |
| ENST00000462388.5:n.183+3A>G | ||
| ENST00000467940.5:c.*415+3A>G | ENSP00000436478.1:n.*415+3A>G | |
| ENST00000470256.5:c.379+3A>G | ENSP00000434985.1:n.379+3A>G | |
| ENST00000475516.5:c.*305+3A>G | ENSP00000433843.1:n.*305+3A>G | |
| ENST00000478796.5:n.479+3A>G | ||
| ENST00000479746.6:n.778A>G | ||
| ENST00000481139.5:n.968A>G | ||
| ENST00000481571.5:c.*305+3A>G | ENSP00000436597.1:n.*305+3A>G | |
| ENST00000483642.5:n.1007+3A>G | ||
| ENST00000485484.5:n.796A>G | ||
| ENST00000488731.6:c.187+3A>G | ENSP00000432330.1:n.187+3A>G | |
| ENST00000492494.5:n.889+3A>G | ||
| ENST00000525160.5:c.*143+3A>G | ENSP00000431568.1:n.*143+3A>G | |
| ENST00000528013.6:c.534+3A>G | ENSP00000433130.2:n.534+3A>G | |
| ENST00000529984.5:c.187+3A>G | ENSP00000437093.1:n.187+3A>G | |
| ENST00000531105.5:c.115+1631A>G | ENSP00000431292.1:n.115+1631A>G | |
| ENST00000533178.5:c.122-73A>G | ENSP00000436430.1:n.122-73A>G | |
| NM_001048171.1:c.534+3A>G | NP_001041636.1:n.534+3A>G | |
| NM_001048172.1:c.495+3A>G | NP_001041637.1:n.495+3A>G | |
| NM_001048173.1:c.492+3A>G | NP_001041638.1:n.492+3A>G | |
| NM_001048174.1:c.492+3A>G | NP_001041639.1:n.492+3A>G | |
| NM_001128425.1:c.576+3A>G , LRG_220t1:c.576+3A>G | NP_001121897.1:n.576+3A>G | |
| NM_001293190.1:c.537+3A>G | NP_001280119.1:n.537+3A>G | |
| NM_001293191.1:c.525+3A>G | NP_001280120.1:n.525+3A>G | |
| NM_001293192.1:c.216+3A>G | NP_001280121.1:n.216+3A>G | |
| NM_001293195.1:c.492+3A>G | NP_001280124.1:n.492+3A>G | |
| NM_001293196.1:c.216+3A>G | NP_001280125.1:n.216+3A>G | |
| NM_012222.2:c.567+3A>G | NP_036354.1:n.567+3A>G | |
| XM_011541497.1:c.552+3A>G | XP_011539799.1:n.552+3A>G | |
| XM_011541498.1:c.534+3A>G | XP_011539800.1:n.534+3A>G | |
| XM_011541499.1:c.534+3A>G | XP_011539801.1:n.534+3A>G | |
| XM_011541500.1:c.534+3A>G | XP_011539802.1:n.534+3A>G | |
| XM_011541501.1:c.534+3A>G | XP_011539803.1:n.534+3A>G | |
| XM_011541502.1:c.534+3A>G | XP_011539804.1:n.534+3A>G | |
| XM_011541503.1:c.534+3A>G | XP_011539805.1:n.534+3A>G | |
| XM_011541504.1:c.525+3A>G | XP_011539806.1:n.525+3A>G | |
| XM_011541505.1:c.114+3A>G | XP_011539807.1:n.114+3A>G | |
| XM_011541506.1:c.114+3A>G | XP_011539808.1:n.114+3A>G | |
| XM_011541507.1:c.105+3A>G | XP_011539809.1:n.105+3A>G | |
| XM_011541508.1:c.120+3A>G | XP_011539810.1:n.120+3A>G | |
| XR_946658.1:n.623+3A>G | ||
| NM_001350650.1:c.147+3A>G | NP_001337579.1:n.147+3A>G | |
| NM_001350651.1:c.147+3A>G | NP_001337580.1:n.147+3A>G | |
| NR_146882.1:n.750+3A>G | ||
| NR_146883.1:n.564+3A>G | ||
| XM_011541497.3:c.552+3A>G | XP_011539799.1:n.552+3A>G | |
| XM_011541500.3:c.534+3A>G | XP_011539802.1:n.534+3A>G | |
| XM_011541501.2:c.534+3A>G | XP_011539803.1:n.534+3A>G | |
| XM_011541502.2:c.534+3A>G | XP_011539804.1:n.534+3A>G | |
| XM_011541503.2:c.534+3A>G | XP_011539805.1:n.534+3A>G | |
| XM_011541504.2:c.525+3A>G | XP_011539806.1:n.525+3A>G | |
| XM_011541505.2:c.114+3A>G | XP_011539807.1:n.114+3A>G | |
| XM_011541506.2:c.114+3A>G | XP_011539808.1:n.114+3A>G | |
| XM_017001331.1:c.534+3A>G | XP_016856820.1:n.534+3A>G | |
| XM_017001332.1:c.534+3A>G | XP_016856821.1:n.534+3A>G | |
| XM_017001333.1:c.534+3A>G | XP_016856822.1:n.534+3A>G | |
| XM_017001334.1:c.495+3A>G | XP_016856823.1:n.495+3A>G | |
| XM_017001335.1:c.216+3A>G | XP_016856824.1:n.216+3A>G | |
| XM_017001336.1:c.147+3A>G | XP_016856825.1:n.147+3A>G | |
| XM_017001337.1:c.147+3A>G | XP_016856826.1:n.147+3A>G | |
| XM_024447244.1:c.147+3A>G | XP_024303012.1:n.147+3A>G | |
| XM_024447245.1:c.147+3A>G | XP_024303013.1:n.147+3A>G | |
| XM_024447248.1:c.105+3A>G | XP_024303016.1:n.105+3A>G | |
| XM_024447249.1:c.-25+3A>G | XP_024303017.1:n.-25+3A>G | |
| XM_024447250.1:c.-25+3A>G | XP_024303018.1:n.-25+3A>G | |
| XM_024447251.1:c.-25+3A>G | XP_024303019.1:n.-25+3A>G | |
| XR_001737190.1:n.537+3A>G | ||
| XR_001737192.1:n.349+3A>G | ||
| XR_002956643.1:n.529+3A>G | ||
| XR_002956644.1:n.1064+3A>G | ||
| XR_946658.2:n.637+3A>G | ||
| NM_001048171.2:c.492+3A>G | NP_001041636.2:n.492+3A>G | |
| NM_001128425.2:c.576+3A>G MANE Plus Clinical | NP_001121897.1:n.576+3A>G | |
| NM_001048172.2:c.495+3A>G | NP_001041637.1:n.495+3A>G | |
| NM_001048173.2:c.492+3A>G | NP_001041638.1:n.492+3A>G | |
| NM_001048174.2:c.492+3A>G MANE Select | NP_001041639.1:n.492+3A>G | |
| NM_001293190.2:c.537+3A>G | NP_001280119.1:n.537+3A>G | |
| NM_001293191.2:c.525+3A>G | NP_001280120.1:n.525+3A>G | |
| NM_001293192.2:c.216+3A>G | NP_001280121.1:n.216+3A>G | |
| NM_001293195.2:c.492+3A>G | NP_001280124.1:n.492+3A>G | |
| NM_001293196.2:c.216+3A>G | NP_001280125.1:n.216+3A>G | |
| NM_001350650.2:c.147+3A>G | NP_001337579.1:n.147+3A>G | |
| NM_001350651.2:c.147+3A>G | NP_001337580.1:n.147+3A>G | |
| NM_012222.3:c.567+3A>G | NP_036354.1:n.567+3A>G | |
| NR_146882.2:n.720+3A>G | ||
| NR_146883.2:n.569+3A>G |