HGVS | Genome Assembly |
---|---|
NC_000005.10:g.141515019A>T , CM000667.2:g.141515019A>T | GRCh38 |
NC_000005.9:g.140894586A>T , CM000667.1:g.140894586A>T | GRCh37 |
NC_000005.8:g.140874770A>T | NCBI36 |
NG_011594.1:g.109037T>A | |
NG_011594.2:g.109037T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389054.7:c.*1832T>A | ENSP00000373706.4:n.*1832T>A | |
ENST00000476339.1:n.2603T>A | ||
XM_011537572.1:c.*1832T>A | XP_011535874.1:n.*1832T>A | |
XM_011537573.1:c.*1832T>A | XP_011535875.1:n.*1832T>A | |
XM_024454384.1:c.*1832T>A | XP_024310152.1:n.*1832T>A | |
XM_024454385.1:c.*1832T>A | XP_024310153.1:n.*1832T>A | |
XM_024454386.1:c.*1832T>A | XP_024310154.1:n.*1832T>A | |
XM_024454387.1:c.*1832T>A | XP_024310155.1:n.*1832T>A |