Canonical Allele Identifier: CA1931509298

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99817342T= , CM000672.2:g.99817342T=	GRCh38
NC_000010.10:g.101577099T= , CM000672.1:g.101577099T=	GRCh37
NC_000010.9:g.101567089T=	NCBI36
NG_011798.1:g.39637T=
NG_011798.2:g.39745T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2129T= MANE Select	ENSP00000497274.1:p.Ile710=
ENST00000370449.8:c.2129T=	ENSP00000359478.4:p.Ile710=
NM_000392.4:c.2129T=	NP_000383.1:p.Ile710=
XM_006717630.2:c.1433T=	XP_006717693.1:p.Ile478=
XM_006717631.2:c.2129T=	XP_006717694.1:p.Ile710=
XM_011539291.1:c.2129T=	XP_011537593.1:p.Ile710=
XR_945604.1:n.2318T=
XR_945605.1:n.2320T=
NM_000392.5:c.2129T= MANE Select	NP_000383.2:p.Ile710=
XM_006717630.3:c.1433T=	XP_006717693.1:p.Ile478=
XM_006717631.4:c.2129T=	XP_006717694.1:p.Ile710=
XM_011539291.3:c.2129T=	XP_011537593.1:p.Ile710=
XM_017015675.2:c.2129T=	XP_016871164.1:p.Ile710=
XR_945604.3:n.2372T=
XR_945605.3:n.2372T=