Linked Data
dbSNP Id:
rs745362323
ExAC:
16:27374149 A / G
gnomAD v2:
16-27374149-A-G
gnomAD v4:
16-27362828-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.27362828A>G , CM000678.2:g.27362828A>G | GRCh38 |
| NC_000016.9:g.27374149A>G , CM000678.1:g.27374149A>G | GRCh37 |
| NC_000016.8:g.27281650A>G | NCBI36 |
| NG_012086.1:g.53899A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395762.7:c.1476A>G MANE Select | ENSP00000379111.2:p.Ala492= | |
| ENST00000170630.6:c.1431A>G | ENSP00000170630.3:p.Ala477= | |
| ENST00000395762.6:c.1476A>G | ENSP00000379111.2:p.Ala492= | |
| ENST00000543915.6:c.1476A>G | ENSP00000441667.2:p.Ala492= | |
| ENST00000565352.1:c.230-1275A>G | ENSP00000461268.1:n.230-1275A>G | |
| ENST00000568746.5:c.*1519A>G | ENSP00000455714.1:n.*1519A>G | |
| NM_000418.3:c.1476A>G | NP_000409.1:p.Ala492= | |
| NM_001257406.1:c.1476A>G | NP_001244335.1:p.Ala492= | |
| NM_001257407.1:c.1431A>G | NP_001244336.1:p.Ala477= | |
| NM_001257997.1:c.996A>G | NP_001244926.1:p.Ala332= | |
| XM_005255308.2:c.585A>G | XP_005255365.1:p.Ala195= | |
| XM_006721043.1:c.525A>G | XP_006721106.1:p.Ala175= | |
| XM_011545825.1:c.1476A>G | XP_011544127.1:p.Ala492= | |
| XM_011545826.1:c.1476A>G | XP_011544128.1:p.Ala492= | |
| XM_011545827.1:c.1476A>G | XP_011544129.1:p.Ala492= | |
| XM_011545828.1:c.1209A>G | XP_011544130.1:p.Ala403= | |
| XM_011545829.1:c.1179A>G | XP_011544131.1:p.Ala393= | |
| XM_011545830.1:c.1179A>G | XP_011544132.1:p.Ala393= | |
| XM_011545831.1:c.1179A>G | XP_011544133.1:p.Ala393= | |
| XM_011545832.1:c.1179A>G | XP_011544134.1:p.Ala393= | |
| XM_011545833.1:c.1179A>G | XP_011544135.1:p.Ala393= | |
| XM_011545834.1:c.1053A>G | XP_011544136.1:p.Ala351= | |
| XM_011545826.2:c.1476A>G | XP_011544128.1:p.Ala492= | |
| XM_011545827.2:c.1476A>G | XP_011544129.1:p.Ala492= | |
| XM_011545828.2:c.1209A>G | XP_011544130.1:p.Ala403= | |
| XM_011545830.2:c.1179A>G | XP_011544132.1:p.Ala393= | |
| XM_011545833.2:c.1179A>G | XP_011544135.1:p.Ala393= | |
| XM_011545834.2:c.1053A>G | XP_011544136.1:p.Ala351= | |
| XM_017023211.1:c.*511A>G | XP_016878700.1:n.*511A>G | |
| NM_000418.4:c.1476A>G MANE Select | NP_000409.1:p.Ala492= | |
| NM_001257406.2:c.1476A>G | NP_001244335.1:p.Ala492= | |
| NM_001257407.2:c.1431A>G | NP_001244336.1:p.Ala477= | |
| NM_001257997.2:c.996A>G | NP_001244926.1:p.Ala332= |