Canonical Allele Identifier: CA471135682

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101605513C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845756C>A , CM000672.2:g.99845756C>A	GRCh38
NC_000010.10:g.101605513C>A , CM000672.1:g.101605513C>A	GRCh37
NC_000010.9:g.101595503C>A	NCBI36
NG_011798.1:g.68051C>A
NG_011798.2:g.68159C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4120C>A MANE Select	ENSP00000497274.1:p.Arg1374=
ENST00000648523.1:c.8C>A
ENST00000649459.1:n.468C>A
ENST00000370449.8:c.4120C>A	ENSP00000359478.4:p.Arg1374=
NM_000392.4:c.4120C>A	NP_000383.1:p.Arg1374=
XM_006717630.2:c.3424C>A	XP_006717693.1:p.Arg1142=
XR_945604.1:n.4250C>A
XR_945605.1:n.4184C>A
NM_000392.5:c.4120C>A MANE Select	NP_000383.2:p.Arg1374=
XM_006717630.3:c.3424C>A	XP_006717693.1:p.Arg1142=
XR_945604.3:n.4304C>A
XR_945605.3:n.4236C>A