Linked Data
dbSNP Id:
rs576255815
ExAC:
18:44104799 C / A
gnomAD v2:
18-44104799-C-A
gnomAD v4:
18-46524836-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.46524836C>A , CM000680.2:g.46524836C>A | GRCh38 |
| NC_000018.9:g.44104799C>A , CM000680.1:g.44104799C>A | GRCh37 |
| NC_000018.8:g.42358797C>A | NCBI36 |
| NG_016646.1:g.137198G>T | |
| NG_016646.2:g.137198G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300591.11:c.1279G>T | ENSP00000300591.6:p.Ala427Ser | |
| ENST00000579038.6:c.991G>T | ENSP00000463285.1:p.Ala331Ser | |
| ENST00000582408.6:c.1279G>T | ENSP00000461964.1:p.Ala427Ser | |
| ENST00000642948.1:c.4612G>T MANE Select | ENSP00000496347.1:p.Ala1538Ser | |
| ENST00000300591.10:c.1279G>T | ENSP00000300591.6:p.Ala427Ser | |
| ENST00000335730.6:n.3925G>T | ||
| ENST00000441551.6:c.3994G>T | ENSP00000387621.2:p.Ala1332Ser | |
| ENST00000536736.5:c.4612G>T | ENSP00000444586.1:p.Ala1538Ser | |
| ENST00000579038.5:c.991G>T | ENSP00000463285.1:p.Ala331Ser | |
| ENST00000582408.5:c.1279G>T | ENSP00000461964.1:p.Ala427Ser | |
| NM_001145472.2:c.1279G>T | NP_001138944.1:p.Ala427Ser | |
| NM_001308013.1:c.991G>T | NP_001294942.1:p.Ala331Ser | |
| NM_144612.6:c.4612G>T | NP_653213.6:p.Ala1538Ser | |
| XM_006722388.2:c.1411G>T | XP_006722451.1:p.Ala471Ser | |
| XM_006722389.2:c.1279G>T | XP_006722452.1:p.Ala427Ser | |
| XM_006722390.2:c.1279G>T | XP_006722453.1:p.Ala427Ser | |
| XM_006722391.2:c.1411G>T | XP_006722454.1:p.Ala471Ser | |
| XM_011525803.1:c.4612G>T | XP_011524105.1:p.Ala1538Ser | |
| XM_011525804.1:c.2773G>T | XP_011524106.1:p.Ala925Ser | |
| XM_011525805.1:c.1276G>T | XP_011524107.1:p.Ala426Ser | |
| XM_011525806.1:c.991G>T | XP_011524108.1:p.Ala331Ser | |
| XM_011525807.1:c.991G>T | XP_011524109.1:p.Ala331Ser | |
| XM_011525809.1:c.991G>T | XP_011524111.1:p.Ala331Ser | |
| XM_006722388.3:c.1411G>T | XP_006722451.1:p.Ala471Ser | |
| XM_006722389.3:c.1279G>T | XP_006722452.1:p.Ala427Ser | |
| XM_006722390.3:c.1279G>T | XP_006722453.1:p.Ala427Ser | |
| XM_006722391.3:c.1411G>T | XP_006722454.1:p.Ala471Ser | |
| XM_011525804.2:c.2773G>T | XP_011524106.1:p.Ala925Ser | |
| XM_017025548.1:c.3994G>T | XP_016881037.1:p.Ala1332Ser | |
| XM_024451084.1:c.3094G>T | XP_024306852.1:p.Ala1032Ser | |
| XM_024451085.1:c.1276G>T | XP_024306853.1:p.Ala426Ser | |
| XM_024451086.1:c.991G>T | XP_024306854.1:p.Ala331Ser | |
| XM_024451087.1:c.991G>T | XP_024306855.1:p.Ala331Ser | |
| XM_024451088.1:c.991G>T | XP_024306856.1:p.Ala331Ser | |
| NM_001145472.3:c.1279G>T | NP_001138944.1:p.Ala427Ser | |
| NM_001308013.2:c.991G>T | NP_001294942.1:p.Ala331Ser | |
| NM_001384474.1:c.4612G>T MANE Select | NP_001371403.1:p.Ala1538Ser | |
| NM_144612.7:c.4612G>T | NP_653213.6:p.Ala1538Ser |