HGVS | Genome Assembly |
---|---|
NC_000004.12:g.3256628G>T , CM000666.2:g.3256628G>T | GRCh38 |
NC_000004.11:g.3258355G>T , CM000666.1:g.3258355G>T | GRCh37 |
NC_000004.10:g.3228153G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000505599.5:c.729+771G>T | ENSP00000425405.1:n.729+771G>T | |
ENST00000510580.1:c.765+735G>T | ENSP00000420966.1:n.765+735G>T | |
XM_011513464.1:c.729+771G>T | XP_011511766.1:n.729+771G>T | |
XR_924950.1:n.753+771G>T |