HGVS | Genome Assembly |
---|---|
NC_000002.12:g.85581864T>C , CM000664.2:g.85581864T>C | GRCh38 |
NC_000002.11:g.85808987T>C , CM000664.1:g.85808987T>C | GRCh37 |
NC_000002.10:g.85662498T>C | NCBI36 |
NG_022887.1:g.9374T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263864.10:c.*148T>C MANE Select | ENSP00000263864.5:n.*148T>C | |
ENST00000263864.9:c.*148T>C | ENSP00000263864.5:n.*148T>C | |
ENST00000409760.1:c.*284T>C | ENSP00000387094.1:n.*284T>C | |
ENST00000432071.1:c.*148T>C | ENSP00000407984.1:n.*148T>C | |
NM_003761.4:c.*148T>C | NP_003752.2:n.*148T>C | |
XM_017005170.1:c.*284T>C | XP_016860659.1:n.*284T>C | |
NM_003761.5:c.*148T>C MANE Select | NP_003752.2:n.*148T>C |