HGVS | Genome Assembly |
---|---|
NC_000010.11:g.78033826C>T , CM000672.2:g.78033826C>T | GRCh38 |
NC_000010.10:g.79793584C>T , CM000672.1:g.79793584C>T | GRCh37 |
NC_000010.9:g.79463590C>T | NCBI36 |
NG_012633.1:g.5067C>T | |
NG_029648.1:g.715G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000613865.5:c.-76C>T | ENSP00000478869.2:n.-76C>T | |
ENST00000435275.5:c.-76C>T | ENSP00000415549.1:n.-76C>T | |
ENST00000440692.5:c.-76C>T | ENSP00000414321.1:n.-76C>T | |
ENST00000613865.4:c.-76C>T | ENSP00000478869.1:n.-76C>T | |
NM_001026.4:c.-76C>T | NP_001017.1:n.-76C>T | |
NM_001142282.1:c.-76C>T | NP_001135754.1:n.-76C>T | |
NM_001142283.1:c.-76C>T | NP_001135755.1:n.-76C>T | |
NM_001142284.1:c.-76C>T | NP_001135756.1:n.-76C>T | |
NM_001142285.1:c.-76C>T | NP_001135757.1:n.-76C>T | |
NM_033022.3:c.-76C>T | NP_148982.1:n.-76C>T |