Canonical Allele Identifier: CA15756620
Gene: ABCC9 HGNC NCBI

Linked Data

dbSNP Id: rs11046205

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21839392G>A , CM000674.2:g.21839392G>A GRCh38
NC_000012.11:g.21992326G>A , CM000674.1:g.21992326G>A GRCh37
NC_000012.10:g.21883593G>A NCBI36
NG_012819.1:g.102303C>T , LRG_377:g.102303C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261200.9:c.3474-1222C>T ENSP00000261200.4:p.=
ENST00000261201.9:n.3474-1222C>T ENSP00000261201.4:p.=
ENST00000261200.8:n.3474-1222C>T ENSP00000261200.4:p.=
ENST00000261201.8:n.3474-1222C>T ENSP00000261201.4:p.=
ENST00000544039.5:n.2355-1222C>T ENSP00000440521.1:p.=
NM_005691.3:c.3474-1222C>T NP_005682.2:p.=
NM_020297.3:c.3474-1222C>T NP_064693.2:p.=
XM_005253284.2:c.3474-1222C>T XP_005253341.1:p.=
XM_005253286.2:c.3474-1222C>T XP_005253343.1:p.=
XM_005253287.3:c.3474-1222C>T XP_005253344.1:p.=
XM_005253288.2:c.3474-1222C>T XP_005253345.1:p.=
XM_005253289.2:c.3435-1222C>T XP_005253346.1:p.=
XM_005253290.2:c.3333-1222C>T XP_005253347.1:p.=
XM_006719025.2:c.3435-1222C>T XP_006719088.1:p.=
XM_011520545.1:c.3474-1222C>T XP_011518847.1:p.=
XM_005253284.4:c.3474-1222C>T XP_005253341.1:p.=
XM_005253286.4:c.3474-1222C>T XP_005253343.1:p.=
XM_005253287.5:c.3474-1222C>T XP_005253344.1:p.=
XM_005253288.4:c.3474-1222C>T XP_005253345.1:p.=
XM_005253289.4:c.3435-1222C>T XP_005253346.1:p.=
XM_005253290.4:c.3333-1222C>T XP_005253347.1:p.=
XM_006719025.4:c.3435-1222C>T XP_006719088.1:p.=
XM_011520545.3:c.3474-1222C>T XP_011518847.1:p.=
NM_001377273.1:c.3474-1222C>T NP_001364202.1:p.=
NM_001377274.1:c.2607-1222C>T NP_001364203.1:p.=
NM_005691.4:c.3474-1222C>T NP_005682.2:p.=
NM_020297.4:c.3474-1222C>T NP_064693.2:p.=