Linked Data
gnomAD v4:
4-99352856-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99352856C>A , CM000666.2:g.99352856C>A | GRCh38 |
| NC_000004.11:g.100274013C>A , CM000666.1:g.100274013C>A | GRCh37 |
| NC_000004.10:g.100493036C>A | NCBI36 |
| NG_011718.1:g.4905G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000515683.5:c.-181G>T | ENSP00000426083.1:n.-181G>T | |
| NM_000669.4:c.-181G>T | NP_000660.1:n.-181G>T | |
| NR_133005.1:n.190G>T | ||
| XM_011531588.1:c.-181G>T | XP_011529890.1:n.-181G>T | |
| XM_011531589.1:c.-421G>T | XP_011529891.1:n.-421G>T |