Linked Data
gnomAD v4:
4-185143311-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.185143311G>A , CM000666.2:g.185143311G>A | GRCh38 |
| NC_000004.11:g.186064465G>A , CM000666.1:g.186064465G>A | GRCh37 |
| NC_000004.10:g.186301459G>A | NCBI36 |
| NG_013001.1:g.5049G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000281456.11:c.-62G>A MANE Select | ENSP00000281456.5:n.-62G>A | |
| ENST00000281456.10:c.-62G>A | ENSP00000281456.5:n.-62G>A | |
| ENST00000491736.1:c.-62G>A | ENSP00000476711.1:n.-62G>A | |
| NM_001151.3:c.-62G>A | NP_001142.2:n.-62G>A | |
| NM_001151.4:c.-62G>A MANE Select | NP_001142.2:n.-62G>A |