HGVS | Genome Assembly |
---|---|
NC_000005.10:g.155875572G>T , CM000667.2:g.155875572G>T | GRCh38 |
NC_000005.9:g.155302582G>T , CM000667.1:g.155302582G>T | GRCh37 |
NC_000005.8:g.155235160G>T | NCBI36 |
NG_008693.2:g.10229G>T , LRG_205:g.10229G>T |
HGVS | Amino-acid Change |
---|---|
ENST00000517913.5:c.-282+5148G>T | ENSP00000429378.1:n.-282+5148G>T |
XM_017009723.2:c.-208+5148G>T | XP_016865212.1:n.-208+5148G>T |
XM_017009724.1:c.-208+146582G>T | XP_016865213.1:n.-208+146582G>T |