Linked Data
gnomAD v4:
4-99353029-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99353029G>T , CM000666.2:g.99353029G>T | GRCh38 |
| NC_000004.11:g.100274186G>T , CM000666.1:g.100274186G>T | GRCh37 |
| NC_000004.10:g.100493209G>T | NCBI36 |
| NG_011718.1:g.4732C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NM_000669.4:c.-354C>A | NP_000660.1:n.-354C>A | |
| NR_133005.1:n.17C>A | ||
| XM_011531589.1:c.-594C>A | XP_011529891.1:n.-594C>A |