HGVS | Genome Assembly |
---|---|
NC_000007.14:g.74789343G>T , CM000669.2:g.74789343G>T | GRCh38 |
NC_000007.13:g.74203687G>T , CM000669.1:g.74203687G>T | GRCh37 |
NC_000007.12:g.73841623G>T | NCBI36 |
NG_009078.2:g.20380G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000289473.10:c.*183G>T | ENSP00000289473.4:n.*183G>T | |
NM_000265.5:c.*183G>T | NP_000256.4:n.*183G>T | |
XM_005250543.3:c.*277G>T | XP_005250600.2:n.*277G>T | |
XM_011516498.1:c.*230G>T | XP_011514800.1:n.*230G>T | |
XM_011516501.1:c.*183G>T | XP_011514803.1:n.*183G>T | |
NM_000265.6:c.*183G>T | NP_000256.4:n.*183G>T |