Canonical Allele Identifier: CA260095
Gene: ABCC9 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 35536
ClinVar RCV Id: RCV000029191
dbSNP Id: rs387907230

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21933888G>A , CM000674.2:g.21933888G>A GRCh38
NC_000012.11:g.22086822G>A , CM000674.1:g.22086822G>A GRCh37
NC_000012.10:g.21978089G>A NCBI36
NG_012819.1:g.7807C>T , LRG_377:g.7807C>T

Transcript Alleles

HGVS Amino-acid change
NM_005691.3:c.178C>T VV NP_005682.2:p.His60Tyr
NM_020297.3:c.178C>T VV NP_064693.2:p.His60Tyr
XM_005253284.2:c.178C>T XP_005253341.1:p.His60Tyr
XM_005253286.2:c.178C>T XP_005253343.1:p.His60Tyr
XM_005253287.3:c.178C>T XP_005253344.1:p.His60Tyr
XM_005253288.2:c.178C>T XP_005253345.1:p.His60Tyr
XM_005253289.2:c.178C>T XP_005253346.1:p.His60Tyr
XM_005253290.2:c.178C>T XP_005253347.1:p.His60Tyr
XM_006719025.2:c.178C>T XP_006719088.1:p.His60Tyr
XM_011520545.1:c.178C>T XP_011518847.1:p.His60Tyr
XM_005253284.4:c.178C>T
XM_005253286.4:c.178C>T
XM_005253287.5:c.178C>T
XM_005253288.4:c.178C>T
XM_005253289.4:c.178C>T
XM_005253290.4:c.178C>T
XM_006719025.4:c.178C>T
XM_011520545.3:c.178C>T
ENST00000261200.8:n.178C>T ENSP00000261200.4:p.His60Tyr
ENST00000261201.8:n.178C>T ENSP00000261201.4:p.His60Tyr
ENST00000326684.8:c.178C>T ENSP00000317518.4:p.His60Tyr
ENST00000538350.5:c.178C>T ENSP00000442604.1:p.His60Tyr
ENST00000621589.1:n.178C>T ENSP00000480233.1:p.His60Tyr