HGVS | Genome Assembly |
---|---|
NC_000014.9:g.73136422A>T , CM000676.2:g.73136422A>T | GRCh38 |
NC_000014.8:g.73603130A>T , CM000676.1:g.73603130A>T | GRCh37 |
NC_000014.7:g.72672883A>T | NCBI36 |
NG_007386.2:g.4952A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000557356.5:c.-162A>T | ENSP00000451498.1:n.-162A>T |