HGVS | Genome Assembly |
---|---|
NC_000011.10:g.61865703G>A , CM000673.2:g.61865703G>A | GRCh38 |
NC_000011.9:g.61633175G>A , CM000673.1:g.61633175G>A | GRCh37 |
NC_000011.8:g.61389751G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000278840.9:c.*14G>A MANE Select | ENSP00000278840.4:n.*14G>A | |
ENST00000257261.10:c.*14G>A | ENSP00000257261.6:n.*14G>A | |
ENST00000278840.8:c.*14G>A | ENSP00000278840.4:n.*14G>A | |
ENST00000522056.5:c.*14G>A | ENSP00000429500.1:n.*14G>A | |
ENST00000523235.5:n.3429G>A | ||
NM_001281501.1:c.*14G>A | NP_001268430.1:n.*14G>A | |
NM_001281502.1:c.*14G>A | NP_001268431.1:n.*14G>A | |
NM_004265.3:c.*14G>A | NP_004256.1:n.*14G>A | |
NM_004265.4:c.*14G>A MANE Select | NP_004256.1:n.*14G>A |