Linked Data
gnomAD v4:
7-74789370-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.74789370A>G , CM000669.2:g.74789370A>G | GRCh38 |
| NC_000007.13:g.74203714A>G , CM000669.1:g.74203714A>G | GRCh37 |
| NC_000007.12:g.73841650A>G | NCBI36 |
| NG_009078.2:g.20407A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289473.10:c.*210A>G | ENSP00000289473.4:n.*210A>G | |
| NM_000265.5:c.*210A>G | NP_000256.4:n.*210A>G | |
| XM_005250543.3:c.*304A>G | XP_005250600.2:n.*304A>G | |
| XM_011516498.1:c.*257A>G | XP_011514800.1:n.*257A>G | |
| XM_011516501.1:c.*210A>G | XP_011514803.1:n.*210A>G | |
| NM_000265.6:c.*210A>G | NP_000256.4:n.*210A>G |