HGVS | Genome Assembly |
---|---|
NC_000001.11:g.147773399T>C , CM000663.2:g.147773399T>C | GRCh38 |
NC_000001.10:g.147245503T>C , CM000663.1:g.147245503T>C | GRCh37 |
NC_000001.9:g.145712127T>C | NCBI36 |
NG_009369.2:g.4976A>G |
HGVS | Amino-acid change | |
---|---|---|
XM_005272951.3:c.-34+7268A>G | XP_005273008.1:n.-34+7268A>G | |
XM_011509415.1:c.-2326A>G | XP_011507717.1:n.-2326A>G | |
XR_922078.1:n.434-4162T>C | ||
XR_922079.1:n.434-4162T>C | ||
XM_005272951.4:c.-34+7268A>G | XP_005273008.1:n.-34+7268A>G | |
XM_017001044.1:c.-2167A>G | XP_016856533.1:n.-2167A>G | |
XR_922079.3:n.744-4162T>C |