HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67947557C>T , CM000673.2:g.67947557C>T | GRCh38 |
NC_000011.9:g.67715028C>T , CM000673.1:g.67715028C>T | GRCh37 |
NC_000011.8:g.67471604C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000527543.2:n.322-7783G>A | ||
XM_024448784.1:c.466-7783G>A | XP_024304552.1:n.466-7783G>A | |
XR_002957254.1:n.1090-7783G>A | ||
XR_002957255.1:n.1085+7925G>A | ||
XR_002957256.1:n.1093-7783G>A |