Linked Data
ClinVar Variation Id:
493260
ClinVar RCV Id:
RCV000585527
dbSNP Id:
rs949615251
gnomAD v4:
19-38565125-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38565125G>A , CM000681.2:g.38565125G>A | GRCh38 |
| NC_000019.9:g.39055765G>A , CM000681.1:g.39055765G>A | GRCh37 |
| NC_000019.8:g.43747605G>A | NCBI36 |
| NG_008866.1:g.136426G>A , LRG_766:g.136426G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000688602.1:c.1201G>A | ||
| ENST00000689936.1:c.1183G>A | ||
| ENST00000359596.8:c.12791G>A MANE Select | ENSP00000352608.2:p.Gly4264Asp | |
| ENST00000355481.8:c.12776G>A | ENSP00000347667.3:p.Gly4259Asp | |
| ENST00000359596.7:c.12791G>A | ENSP00000352608.2:p.Gly4264Asp | |
| ENST00000360985.7:c.12773G>A | ENSP00000354254.4:p.Gly4258Asp | |
| ENST00000594335.5:c.6160G>A | ||
| NM_000540.2:c.12791G>A , LRG_766t1:c.12791G>A | NP_000531.2:p.Gly4264Asp | |
| NM_001042723.1:c.12776G>A | NP_001036188.1:p.Gly4259Asp | |
| XM_006723317.1:c.12773G>A | XP_006723380.1:p.Gly4258Asp | |
| XM_006723319.1:c.12758G>A | XP_006723382.1:p.Gly4253Asp | |
| XM_011527204.1:c.12788G>A | XP_011525506.1:p.Gly4263Asp | |
| XM_011527205.1:c.12791G>A | XP_011525507.1:p.Gly4264Asp | |
| XM_006723317.2:c.12773G>A | XP_006723380.1:p.Gly4258Asp | |
| XM_006723319.2:c.12758G>A | XP_006723382.1:p.Gly4253Asp | |
| XM_011527205.2:c.12791G>A | XP_011525507.1:p.Gly4264Asp | |
| NM_000540.3:c.12791G>A MANE Select | NP_000531.2:p.Gly4264Asp | |
| NM_001042723.2:c.12776G>A | NP_001036188.1:p.Gly4259Asp |