HGVS | Genome Assembly |
---|---|
NC_000012.12:g.56450191C>A , CM000674.2:g.56450191C>A | GRCh38 |
NC_000012.11:g.56843975C>A , CM000674.1:g.56843975C>A | GRCh37 |
NC_000012.10:g.55130242C>A | NCBI36 |
NG_021397.1:g.9461G>T | |
NG_021397.2:g.23976G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648304.1:c.*1505G>T | ENSP00000497190.1:n.*1505G>T | |
ENST00000652304.1:c.*1089G>T MANE Select | ENSP00000498622.1:n.*1089G>T | |
ENST00000257979.4:c.*1089G>T | ENSP00000257979.4:n.*1089G>T | |
NM_012064.3:c.*1089G>T | NP_036196.1:n.*1089G>T | |
XM_011538354.1:c.*1089G>T | XP_011536656.1:n.*1089G>T | |
NM_012064.4:c.*1089G>T MANE Select | NP_036196.1:n.*1089G>T | |
XM_017019306.1:c.*1089G>T | XP_016874795.1:n.*1089G>T |