Canonical Allele Identifier: CA471261822

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101578591C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99818834C>A , CM000672.2:g.99818834C>A	GRCh38
NC_000010.10:g.101578591C>A , CM000672.1:g.101578591C>A	GRCh37
NC_000010.9:g.101568581C>A	NCBI36
NG_011798.1:g.41129C>A
NG_011798.2:g.41237C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2316C>A MANE Select	ENSP00000497274.1:p.Ala772=
ENST00000370449.8:c.2316C>A	ENSP00000359478.4:p.Ala772=
NM_000392.4:c.2316C>A	NP_000383.1:p.Ala772=
XM_006717630.2:c.1620C>A	XP_006717693.1:p.Ala540=
XM_006717631.2:c.2316C>A	XP_006717694.1:p.Ala772=
XM_011539291.1:c.2316C>A	XP_011537593.1:p.Ala772=
XR_945604.1:n.2505C>A
XR_945605.1:n.2507C>A
NM_000392.5:c.2316C>A MANE Select	NP_000383.2:p.Ala772=
XM_006717630.3:c.1620C>A	XP_006717693.1:p.Ala540=
XM_006717631.4:c.2316C>A	XP_006717694.1:p.Ala772=
XM_011539291.3:c.2316C>A	XP_011537593.1:p.Ala772=
XM_017015675.2:c.2316C>A	XP_016871164.1:p.Ala772=
XR_945604.3:n.2559C>A
XR_945605.3:n.2559C>A