Canonical Allele Identifier: CA233619497

Gene: ABCC9

Linked Data

• dbSNP Id: rs939526271
• MyVariant Identifiers: chr12:g.22078224T>C (hg19) ; chr12:g.21925290T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21925290T>C , CM000674.2:g.21925290T>C	GRCh38
NC_000012.11:g.22078224T>C , CM000674.1:g.22078224T>C	GRCh37
NC_000012.10:g.21969491T>C	NCBI36
NG_012819.1:g.16405A>G , LRG_377:g.16405A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261201.10:c.406+652A>G	ENSP00000261201.4:n.406+652A>G
ENST00000621589.2:c.406+652A>G	ENSP00000480233.1:n.406+652A>G
ENST00000682068.1:c.406+652A>G	ENSP00000507226.1:n.406+652A>G
ENST00000682646.1:n.1314A>G
ENST00000682789.1:n.657+652A>G
ENST00000682879.1:c.406+652A>G	ENSP00000508210.1:n.406+652A>G
ENST00000683105.1:c.406+652A>G	ENSP00000506801.1:n.406+652A>G
ENST00000683676.1:c.406+652A>G	ENSP00000508167.1:n.406+652A>G
ENST00000684084.1:c.406+652A>G	ENSP00000507859.1:n.406+652A>G
ENST00000684435.1:c.*566A>G	ENSP00000507779.1:n.*566A>G
ENST00000684543.1:n.751+652A>G
ENST00000261200.9:c.406+652A>G MANE Select	ENSP00000261200.4:n.406+652A>G
ENST00000261201.9:c.406+652A>G	ENSP00000261201.4:n.406+652A>G
ENST00000636888.1:c.406+652A>G	ENSP00000490640.1:n.406+652A>G
ENST00000261200.8:c.406+652A>G	ENSP00000261200.4:n.406+652A>G
ENST00000261201.8:c.406+652A>G	ENSP00000261201.4:n.406+652A>G
ENST00000326684.8:c.406+652A>G	ENSP00000317518.4:n.406+652A>G
ENST00000538350.5:c.*163A>G	ENSP00000442604.1:n.*163A>G
ENST00000621589.1:c.406+652A>G	ENSP00000480233.1:n.406+652A>G
NM_005691.3:c.406+652A>G	NP_005682.2:n.406+652A>G
NM_020297.3:c.406+652A>G	NP_064693.2:n.406+652A>G
XM_005253284.2:c.406+652A>G	XP_005253341.1:n.406+652A>G
XM_005253286.2:c.406+652A>G	XP_005253343.1:n.406+652A>G
XM_005253287.3:c.406+652A>G	XP_005253344.1:n.406+652A>G
XM_005253288.2:c.406+652A>G	XP_005253345.1:n.406+652A>G
XM_005253289.2:c.406+652A>G	XP_005253346.1:n.406+652A>G
XM_005253290.2:c.406+652A>G	XP_005253347.1:n.406+652A>G
XM_006719025.2:c.406+652A>G	XP_006719088.1:n.406+652A>G
XM_011520545.1:c.406+652A>G	XP_011518847.1:n.406+652A>G
XM_005253284.4:c.406+652A>G	XP_005253341.1:n.406+652A>G
XM_005253286.4:c.406+652A>G	XP_005253343.1:n.406+652A>G
XM_005253287.5:c.406+652A>G	XP_005253344.1:n.406+652A>G
XM_005253288.4:c.406+652A>G	XP_005253345.1:n.406+652A>G
XM_005253289.4:c.406+652A>G	XP_005253346.1:n.406+652A>G
XM_005253290.4:c.406+652A>G	XP_005253347.1:n.406+652A>G
XM_006719025.4:c.406+652A>G	XP_006719088.1:n.406+652A>G
XM_011520545.3:c.406+652A>G	XP_011518847.1:n.406+652A>G
NM_001377273.1:c.406+652A>G	NP_001364202.1:n.406+652A>G
NM_001377274.1:c.-49+652A>G	NP_001364203.1:n.-49+652A>G
NM_005691.4:c.406+652A>G	NP_005682.2:n.406+652A>G
NM_020297.4:c.406+652A>G MANE Select	NP_064693.2:n.406+652A>G