Linked Data
gnomAD v4:
7-94426486-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94426486G>T , CM000669.2:g.94426486G>T | GRCh38 |
| NC_000007.13:g.94055798G>T , CM000669.1:g.94055798G>T | GRCh37 |
| NC_000007.12:g.93893734G>T | NCBI36 |
| NG_007405.1:g.36926G>T , LRG_2:g.36926G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.3061G>T MANE Select | ENSP00000297268.6:p.Gly1021Cys | |
| ENST00000297268.10:c.3061G>T | ENSP00000297268.6:p.Gly1021Cys | |
| ENST00000478215.1:n.620G>T | ||
| ENST00000481570.5:n.3034G>T | ||
| ENST00000620463.1:c.3055G>T | ENSP00000477719.1:p.Gly1019Cys | |
| NM_000089.3:c.3061G>T , LRG_2t1:c.3061G>T | NP_000080.2:p.Gly1021Cys | |
| NM_000089.4:c.3061G>T MANE Select | NP_000080.2:p.Gly1021Cys |