Linked Data
gnomAD v4:
11-6390400-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6390400G>T , CM000673.2:g.6390400G>T | GRCh38 |
| NC_000011.9:g.6411630G>T , CM000673.1:g.6411630G>T | GRCh37 |
| NC_000011.8:g.6368206G>T | NCBI36 |
| NG_011780.1:g.4976G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_005253075.3:c.-199G>T | XP_005253132.1:n.-199G>T | |
| XM_011520303.1:c.-199G>T | XP_011518605.1:n.-199G>T | |
| XM_011520304.1:c.-199G>T | XP_011518606.1:n.-199G>T | |
| XR_930886.1:n.100G>T |