Linked Data
ClinVar Variation Id:
387417
dbSNP Id:
rs368995122
ExAC:
14:105180602 G / A
gnomAD v2:
14-105180602-G-A
gnomAD v3:
14-104714265-G-A
gnomAD v4:
14-104714265-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.104714265G>A , CM000676.2:g.104714265G>A | GRCh38 |
| NC_000014.8:g.105180602G>A , CM000676.1:g.105180602G>A | GRCh37 |
| NC_000014.7:g.104251647G>A | NCBI36 |
| NG_027684.1:g.29660G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392634.9:c.3103G>A MANE Select | ENSP00000376410.4:p.Gly1035Ser | |
| ENST00000617571.5:c.3099G>A | ENSP00000483829.2:p.Pro1033= | |
| ENST00000674520.1:c.3098G>A | ENSP00000502593.1:n.3098G>A | |
| ENST00000674631.1:c.1141G>A | ENSP00000502830.1:p.Gly381Ser | |
| ENST00000674662.1:c.3107G>A | ENSP00000501895.1:n.3107G>A | |
| ENST00000674757.1:c.3108G>A | ENSP00000502202.1:p.Pro1036= | |
| ENST00000674822.1:c.2987G>A | ENSP00000501552.1:n.2987G>A | |
| ENST00000674846.1:c.3098G>A | ENSP00000502431.1:n.3098G>A | |
| ENST00000674857.1:c.3092G>A | ENSP00000501687.1:n.3092G>A | |
| ENST00000674960.1:c.2961G>A | ENSP00000501841.1:n.2961G>A | |
| ENST00000674991.1:c.2353G>A | ENSP00000502004.1:p.Gly785Ser | |
| ENST00000675207.1:c.3199G>A | ENSP00000502644.1:p.Gly1067Ser | |
| ENST00000675329.1:c.3079G>A | ENSP00000502287.1:p.Gly1027Ser | |
| ENST00000675481.1:c.3103G>A | ENSP00000502723.1:p.Gly1035Ser | |
| ENST00000675583.1:c.3032G>A | ENSP00000501740.1:n.3032G>A | |
| ENST00000675603.1:n.343G>A | ||
| ENST00000675638.1:c.3041-19G>A | ENSP00000501647.1:n.3041-19G>A | |
| ENST00000675724.1:c.3041G>A | ENSP00000502576.1:n.3041G>A | |
| ENST00000675771.1:c.2366G>A | ENSP00000502104.1:n.2366G>A | |
| ENST00000675797.1:c.2508G>A | ENSP00000502023.1:n.2508G>A | |
| ENST00000675809.1:c.3158G>A | ENSP00000502587.1:n.3158G>A | |
| ENST00000675930.1:c.3103G>A | ENSP00000502456.1:p.Gly1035Ser | |
| ENST00000675980.1:c.3121G>A | ENSP00000502520.1:p.Gly1041Ser | |
| ENST00000676016.1:c.3002G>A | ENSP00000502412.1:n.3002G>A | |
| ENST00000676366.1:c.3103G>A | ENSP00000501605.1:p.Gly1035Ser | |
| ENST00000252527.8:c.1507G>A | ENSP00000252527.8:p.Gly503Ser | |
| ENST00000330634.11:c.3103G>A | ENSP00000376406.3:p.Gly1035Ser | |
| ENST00000392634.8:c.3103G>A | ENSP00000376410.4:p.Gly1035Ser | |
| ENST00000617571.4:c.-1031G>A | ENSP00000483829.1:n.-1031G>A | |
| NM_001031714.3:c.3103G>A | NP_001026884.3:p.Gly1035Ser | |
| NM_022489.3:c.3103G>A | NP_071934.3:p.Gly1035Ser | |
| XM_005268004.3:c.3199G>A | XP_005268061.1:p.Gly1067Ser | |
| XM_005268005.3:c.3199G>A | XP_005268062.1:p.Gly1067Ser | |
| XR_943507.1:n.3328G>A | ||
| XM_005268004.4:c.3199G>A | XP_005268061.1:p.Gly1067Ser | |
| XM_005268005.4:c.3199G>A | XP_005268062.1:p.Gly1067Ser | |
| XM_017021595.1:c.3199G>A | XP_016877084.1:p.Gly1067Ser | |
| NM_001031714.4:c.3103G>A | NP_001026884.3:p.Gly1035Ser | |
| NM_022489.4:c.3103G>A MANE Select | NP_071934.3:p.Gly1035Ser |