Linked Data
gnomAD v4:
11-6390332-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6390332G>T , CM000673.2:g.6390332G>T | GRCh38 |
| NC_000011.9:g.6411562G>T , CM000673.1:g.6411562G>T | GRCh37 |
| NC_000011.8:g.6368138G>T | NCBI36 |
| NG_011780.1:g.4908G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_005253075.3:c.-267G>T | XP_005253132.1:n.-267G>T | |
| XM_011520303.1:c.-267G>T | XP_011518605.1:n.-267G>T | |
| XM_011520304.1:c.-267G>T | XP_011518606.1:n.-267G>T | |
| XR_930886.1:n.32G>T |