Canonical Allele Identifier: CA1931489189

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830389A= , CM000672.2:g.99830389A=	GRCh38
NC_000010.10:g.101590146A= , CM000672.1:g.101590146A=	GRCh37
NC_000010.9:g.101580136A=	NCBI36
NG_011798.1:g.52684A=
NG_011798.2:g.52792A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2703A= MANE Select	ENSP00000497274.1:p.Ile901=
ENST00000370449.8:c.2703A=	ENSP00000359478.4:p.Ile901=
NM_000392.4:c.2703A=	NP_000383.1:p.Ile901=
XM_006717630.2:c.2007A=	XP_006717693.1:p.Ile669=
XM_006717631.2:c.*130A=	XP_006717694.1:n.*130A=
XM_011539291.1:c.2703A=	XP_011537593.1:p.Ile901=
XR_945604.1:n.2892A=
XR_945605.1:n.2894A=
NM_000392.5:c.2703A= MANE Select	NP_000383.2:p.Ile901=
XM_006717630.3:c.2007A=	XP_006717693.1:p.Ile669=
XM_006717631.4:c.*130A=	XP_006717694.1:n.*130A=
XM_011539291.3:c.2703A=	XP_011537593.1:p.Ile901=
XR_945604.3:n.2946A=
XR_945605.3:n.2946A=