HGVS | Genome Assembly |
---|---|
NC_000010.11:g.17129826G>A , CM000672.2:g.17129826G>A | GRCh38 |
NC_000010.10:g.17171825G>A , CM000672.1:g.17171825G>A | GRCh37 |
NC_000010.9:g.17211831G>A | NCBI36 |
NG_008967.1:g.4992C>T , LRG_540:g.4992C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377833.8:c.-61C>T | ENSP00000367064.4:n.-61C>T | |
XM_011519708.1:c.-61C>T | XP_011518010.1:n.-61C>T | |
XM_011519708.2:c.-61C>T | XP_011518010.1:n.-61C>T |