Linked Data
dbSNP Id:
rs748937436
gnomAD v2:
3-119134043-G-A
gnomAD v3:
3-119415196-G-A
gnomAD v4:
3-119415196-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119415196G>A , CM000665.2:g.119415196G>A | GRCh38 |
| NC_000003.11:g.119134043G>A , CM000665.1:g.119134043G>A | GRCh37 |
| NC_000003.10:g.120616733G>A | NCBI36 |
| NG_007665.2:g.125824G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.3267G>A MANE Select | ENSP00000264245.4:p.Gln1089= | |
| ENST00000264245.8:c.3267G>A | ENSP00000264245.4:p.Gln1089= | |
| NM_020754.3:c.3267G>A | NP_065805.2:p.Gln1089= | |
| XM_005247671.3:c.3174G>A | XP_005247728.1:p.Gln1058= | |
| XM_006713714.2:c.3207G>A | XP_006713777.1:p.Gln1069= | |
| XM_006713714.3:c.3207G>A | XP_006713777.1:p.Gln1069= | |
| XM_017006955.1:c.2775G>A | XP_016862444.1:p.Gln925= | |
| NM_020754.4:c.3267G>A MANE Select | NP_065805.2:p.Gln1089= |