HGVS | Genome Assembly |
---|---|
NC_000001.11:g.147773412T>A , CM000663.2:g.147773412T>A | GRCh38 |
NC_000001.10:g.147245516T>A , CM000663.1:g.147245516T>A | GRCh37 |
NC_000001.9:g.145712140T>A | NCBI36 |
NG_009369.2:g.4963A>T |
HGVS | Amino-acid change | |
---|---|---|
XM_005272951.3:c.-34+7255A>T | XP_005273008.1:n.-34+7255A>T | |
XM_011509415.1:c.-2339A>T | XP_011507717.1:n.-2339A>T | |
XR_922078.1:n.434-4149T>A | ||
XR_922079.1:n.434-4149T>A | ||
XM_005272951.4:c.-34+7255A>T | XP_005273008.1:n.-34+7255A>T | |
XM_017001044.1:c.-2180A>T | XP_016856533.1:n.-2180A>T | |
XR_922079.3:n.744-4149T>A |