HGVS | Genome Assembly |
---|---|
NC_000019.10:g.44909395C>T , CM000681.2:g.44909395C>T | GRCh38 |
NC_000019.9:g.45412652C>T , CM000681.1:g.45412652C>T | GRCh37 |
NC_000019.8:g.50104492C>T | NCBI36 |
NG_007084.2:g.8614C>T |
HGVS | Amino-acid Change | |
---|---|---|
NM_000041.3:c.*145C>T | NP_000032.1:n.*145C>T | |
NM_001302688.1:c.*145C>T | NP_001289617.1:n.*145C>T | |
NM_001302689.1:c.*145C>T | NP_001289618.1:n.*145C>T | |
NM_001302690.1:c.*145C>T | NP_001289619.1:n.*145C>T | |
NM_001302691.1:c.*145C>T | NP_001289620.1:n.*145C>T |