HGVS | Genome Assembly |
---|---|
NC_000016.10:g.84544635A>T , CM000678.2:g.84544635A>T | GRCh38 |
NC_000016.9:g.84578241A>T , CM000678.1:g.84578241A>T | GRCh37 |
NC_000016.8:g.83135742A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000565079.5:c.-26+9311T>A | ENSP00000457557.1:n.-26+9311T>A | |
XM_011523250.1:c.-26+9311T>A | XP_011521552.1:n.-26+9311T>A |