MyVariant.info:
GRCh37
chr9:g.133738356G>A
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.130862969G>A , CM000671.2:g.130862969G>A | GRCh38 |
| NC_000009.11:g.133738356G>A , CM000671.1:g.133738356G>A | GRCh37 |
| NC_000009.10:g.132728177G>A | NCBI36 |
| NG_012034.1:g.154089G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372348.9:c.813G>A | ENSP00000361423.2:p.Gln271= | |
| ENST00000318560.6:c.756G>A MANE Select | ENSP00000323315.5:p.Gln252= | |
| ENST00000372348.7:c.813G>A | ENSP00000361423.2:p.Gln271= | |
| ENST00000318560.5:c.756G>A | ENSP00000323315.5:p.Gln252= | |
| ENST00000372348.6:c.813G>A | ENSP00000361423.2:p.Gln271= | |
| NM_005157.5:c.756G>A | NP_005148.2:p.Gln252= | |
| NM_007313.2:c.813G>A | NP_009297.2:p.Gln271= | |
| NM_005157.6:c.756G>A MANE Select | NP_005148.2:p.Gln252= | |
| NM_007313.3:c.813G>A | NP_009297.2:p.Gln271= |