Linked Data
ClinVar Variation Id:
1407584
ClinVar RCV Id:
RCV001918523
dbSNP Id:
rs768829713
ExAC:
3:119101987 G / A
gnomAD v2:
3-119101987-G-A
gnomAD v3:
3-119383140-G-A
gnomAD v4:
3-119383140-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119383140G>A , CM000665.2:g.119383140G>A | GRCh38 |
| NC_000003.11:g.119101987G>A , CM000665.1:g.119101987G>A | GRCh37 |
| NC_000003.10:g.120584677G>A | NCBI36 |
| NG_007665.2:g.93768G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.596G>A MANE Select | ENSP00000264245.4:p.Arg199Gln | |
| ENST00000264245.8:c.596G>A | ENSP00000264245.4:p.Arg199Gln | |
| NM_020754.3:c.596G>A | NP_065805.2:p.Arg199Gln | |
| XM_005247671.3:c.503G>A | XP_005247728.1:p.Arg168Gln | |
| XM_006713714.2:c.596G>A | XP_006713777.1:p.Arg199Gln | |
| XM_006713714.3:c.596G>A | XP_006713777.1:p.Arg199Gln | |
| XM_017006955.1:c.104G>A | XP_016862444.1:p.Arg35Gln | |
| NM_020754.4:c.596G>A MANE Select | NP_065805.2:p.Arg199Gln |