HGVS | Genome Assembly |
---|---|
NC_000001.11:g.185734740T>C , CM000663.2:g.185734740T>C | GRCh38 |
NC_000001.10:g.185703872T>C , CM000663.1:g.185703872T>C | GRCh37 |
NC_000001.9:g.183970495T>C | NCBI36 |
NG_011841.1:g.5190T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271588.9:c.-40T>C MANE Select | ENSP00000271588.4:n.-40T>C | |
ENST00000271588.8:c.-40T>C | ENSP00000271588.4:n.-40T>C | |
NM_031935.2:c.-40T>C | NP_114141.2:n.-40T>C | |
XM_011510037.1:c.-40T>C | XP_011508339.1:n.-40T>C | |
XM_011510038.1:c.-40T>C | XP_011508340.1:n.-40T>C | |
XM_011510039.1:c.-40T>C | XP_011508341.1:n.-40T>C | |
XM_011510040.1:c.-40T>C | XP_011508342.1:n.-40T>C | |
XM_011510041.1:c.-40T>C | XP_011508343.1:n.-40T>C | |
XM_011510038.3:c.-40T>C | XP_011508340.1:n.-40T>C | |
XM_011510041.3:c.-40T>C | XP_011508343.1:n.-40T>C | |
XM_024450118.1:c.-40T>C | XP_024305886.1:n.-40T>C | |
NM_031935.3:c.-40T>C MANE Select | NP_114141.2:n.-40T>C |