Linked Data
ClinVar Variation Id:
161260
dbSNP Id:
rs143388949
ExAC:
4:55573290 A / G
gnomAD v2:
4-55573290-A-G
gnomAD v3:
4-54707124-A-G
gnomAD v4:
4-54707124-A-G
PubMed:
PMID:25637381
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.54707124A>G , CM000666.2:g.54707124A>G | GRCh38 |
| NC_000004.11:g.55573290A>G , CM000666.1:g.55573290A>G | GRCh37 |
| NC_000004.10:g.55268047A>G | NCBI36 |
| NG_007456.1:g.54130A>G , LRG_307:g.54130A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000412167.7:c.955A>G | ENSP00000390987.3:p.Met319Val | |
| ENST00000685269.1:n.1030A>G | ||
| ENST00000685816.1:c.169+3232A>G | ENSP00000508749.1:n.169+3232A>G | |
| ENST00000686011.1:c.952A>G | ENSP00000509704.1:p.Met318Val | |
| ENST00000687109.1:c.955A>G | ENSP00000509371.1:p.Met319Val | |
| ENST00000687208.1:n.1367A>G | ||
| ENST00000687246.1:c.952A>G | ENSP00000509114.1:p.Met318Val | |
| ENST00000687265.1:n.1122A>G | ||
| ENST00000687295.1:c.952A>G | ENSP00000509450.1:p.Met318Val | |
| ENST00000689832.1:c.955A>G | ENSP00000509084.1:p.Met319Val | |
| ENST00000689994.1:c.442A>G | ENSP00000509156.1:p.Met148Val | |
| ENST00000690519.1:c.952A>G | ENSP00000508845.1:p.Met318Val | |
| ENST00000690543.1:c.955A>G | ENSP00000508831.1:p.Met319Val | |
| ENST00000690917.1:n.1170A>G | ||
| ENST00000692783.1:c.952A>G | ENSP00000508733.1:p.Met318Val | |
| ENST00000692991.1:n.1061A>G | ||
| ENST00000288135.6:c.952A>G MANE Select | ENSP00000288135.6:p.Met318Val | |
| ENST00000288135.5:c.952A>G | ENSP00000288135.5:p.Met318Val | |
| ENST00000412167.6:c.952A>G | ENSP00000390987.2:p.Met318Val | |
| NM_000222.2:c.952A>G , LRG_307t1:c.952A>G | NP_000213.1:p.Met318Val | |
| NM_001093772.1:c.952A>G | NP_001087241.1:p.Met318Val | |
| XM_005265740.1:c.955A>G | XP_005265797.1:p.Met319Val | |
| XM_005265741.1:c.955A>G | XP_005265798.1:p.Met319Val | |
| XM_005265742.1:c.955A>G | XP_005265799.1:p.Met319Val | |
| XM_005265742.3:c.955A>G | XP_005265799.1:p.Met319Val | |
| XM_017008178.1:c.952A>G | XP_016863667.1:p.Met318Val | |
| XM_017008179.1:c.955A>G | XP_016863668.1:p.Met319Val | |
| XM_017008180.1:c.952A>G | XP_016863669.1:p.Met318Val | |
| NM_000222.3:c.952A>G MANE Select | NP_000213.1:p.Met318Val | |
| NM_001093772.2:c.952A>G | NP_001087241.1:p.Met318Val | |
| NM_001385284.1:c.955A>G | NP_001372213.1:p.Met319Val | |
| NM_001385285.1:c.952A>G | NP_001372214.1:p.Met318Val | |
| NM_001385286.1:c.952A>G | NP_001372215.1:p.Met318Val | |
| NM_001385288.1:c.955A>G | NP_001372217.1:p.Met319Val | |
| NM_001385290.1:c.955A>G | NP_001372219.1:p.Met319Val | |
| NM_001385292.1:c.955A>G | NP_001372221.1:p.Met319Val |