Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99353045C>T , CM000666.2:g.99353045C>T | GRCh38 |
| NC_000004.11:g.100274202C>T , CM000666.1:g.100274202C>T | GRCh37 |
| NC_000004.10:g.100493225C>T | NCBI36 |
| NG_011718.1:g.4716G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NM_000669.4:c.-370G>A | NP_000660.1:n.-370G>A | |
| NR_133005.1:n.1G>A | ||
| XM_011531589.1:c.-610G>A | XP_011529891.1:n.-610G>A |