HGVS | Genome Assembly |
---|---|
NC_000010.11:g.78033835T>C , CM000672.2:g.78033835T>C | GRCh38 |
NC_000010.10:g.79793593T>C , CM000672.1:g.79793593T>C | GRCh37 |
NC_000010.9:g.79463599T>C | NCBI36 |
NG_012633.1:g.5076T>C | |
NG_029648.1:g.706A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000613865.5:c.-67T>C | ENSP00000478869.2:n.-67T>C | |
ENST00000435275.5:c.-67T>C | ENSP00000415549.1:n.-67T>C | |
ENST00000440692.5:c.-67T>C | ENSP00000414321.1:n.-67T>C | |
ENST00000613865.4:c.-67T>C | ENSP00000478869.1:n.-67T>C | |
NM_001026.4:c.-67T>C | NP_001017.1:n.-67T>C | |
NM_001142282.1:c.-67T>C | NP_001135754.1:n.-67T>C | |
NM_001142283.1:c.-67T>C | NP_001135755.1:n.-67T>C | |
NM_001142284.1:c.-67T>C | NP_001135756.1:n.-67T>C | |
NM_001142285.1:c.-67T>C | NP_001135757.1:n.-67T>C | |
NM_033022.3:c.-67T>C | NP_148982.1:n.-67T>C |