Linked Data
gnomAD v4:
7-94426453-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94426453G>A , CM000669.2:g.94426453G>A | GRCh38 |
| NC_000007.13:g.94055765G>A , CM000669.1:g.94055765G>A | GRCh37 |
| NC_000007.12:g.93893701G>A | NCBI36 |
| NG_007405.1:g.36893G>A , LRG_2:g.36893G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.3028G>A MANE Select | ENSP00000297268.6:p.Glu1010Lys | |
| ENST00000297268.10:c.3028G>A | ENSP00000297268.6:p.Glu1010Lys | |
| ENST00000478215.1:n.587G>A | ||
| ENST00000481570.5:n.3001G>A | ||
| ENST00000620463.1:c.3022G>A | ENSP00000477719.1:p.Glu1008Lys | |
| NM_000089.3:c.3028G>A , LRG_2t1:c.3028G>A | NP_000080.2:p.Glu1010Lys | |
| NM_000089.4:c.3028G>A MANE Select | NP_000080.2:p.Glu1010Lys |