Canonical Allele Identifier: CA478874016

Gene: ABCC9

Linked Data

• MyVariant Identifiers: chr12:g.22086724A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21933790A>C , CM000674.2:g.21933790A>C	GRCh38
NC_000012.11:g.22086724A>C , CM000674.1:g.22086724A>C	GRCh37
NC_000012.10:g.21977991A>C	NCBI36
NG_012819.1:g.7905T>G , LRG_377:g.7905T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261201.10:c.276T>G	ENSP00000261201.4:p.Val92=
ENST00000621589.2:c.276T>G	ENSP00000480233.1:p.Val92=
ENST00000682068.1:c.276T>G	ENSP00000507226.1:p.Val92=
ENST00000682646.1:n.532T>G
ENST00000682789.1:n.527T>G
ENST00000682879.1:c.276T>G	ENSP00000508210.1:p.Val92=
ENST00000683105.1:c.276T>G	ENSP00000506801.1:p.Val92=
ENST00000683676.1:c.276T>G	ENSP00000508167.1:p.Val92=
ENST00000684084.1:c.276T>G	ENSP00000507859.1:p.Val92=
ENST00000684435.1:c.276T>G	ENSP00000507779.1:p.Val92=
ENST00000684543.1:n.621T>G
ENST00000261200.9:c.276T>G MANE Select	ENSP00000261200.4:p.Val92=
ENST00000261201.9:c.276T>G	ENSP00000261201.4:p.Val92=
ENST00000636888.1:c.276T>G	ENSP00000490640.1:p.Val92=
ENST00000261200.8:c.276T>G	ENSP00000261200.4:p.Val92=
ENST00000261201.8:c.276T>G	ENSP00000261201.4:p.Val92=
ENST00000326684.8:c.276T>G	ENSP00000317518.4:p.Val92=
ENST00000538350.5:c.276T>G	ENSP00000442604.1:p.Val92=
ENST00000621589.1:c.276T>G	ENSP00000480233.1:p.Val92=
NM_005691.3:c.276T>G	NP_005682.2:p.Val92=
NM_020297.3:c.276T>G	NP_064693.2:p.Val92=
XM_005253284.2:c.276T>G	XP_005253341.1:p.Val92=
XM_005253286.2:c.276T>G	XP_005253343.1:p.Val92=
XM_005253287.3:c.276T>G	XP_005253344.1:p.Val92=
XM_005253288.2:c.276T>G	XP_005253345.1:p.Val92=
XM_005253289.2:c.276T>G	XP_005253346.1:p.Val92=
XM_005253290.2:c.276T>G	XP_005253347.1:p.Val92=
XM_006719025.2:c.276T>G	XP_006719088.1:p.Val92=
XM_011520545.1:c.276T>G	XP_011518847.1:p.Val92=
XM_005253284.4:c.276T>G	XP_005253341.1:p.Val92=
XM_005253286.4:c.276T>G	XP_005253343.1:p.Val92=
XM_005253287.5:c.276T>G	XP_005253344.1:p.Val92=
XM_005253288.4:c.276T>G	XP_005253345.1:p.Val92=
XM_005253289.4:c.276T>G	XP_005253346.1:p.Val92=
XM_005253290.4:c.276T>G	XP_005253347.1:p.Val92=
XM_006719025.4:c.276T>G	XP_006719088.1:p.Val92=
XM_011520545.3:c.276T>G	XP_011518847.1:p.Val92=
NM_001377273.1:c.276T>G	NP_001364202.1:p.Val92=
NM_001377274.1:c.-179T>G	NP_001364203.1:n.-179T>G
NM_005691.4:c.276T>G	NP_005682.2:p.Val92=
NM_020297.4:c.276T>G MANE Select	NP_064693.2:p.Val92=