Canonical Allele Identifier: CA1931509120

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99817255C= , CM000672.2:g.99817255C=	GRCh38
NC_000010.10:g.101577012C= , CM000672.1:g.101577012C=	GRCh37
NC_000010.9:g.101567002C=	NCBI36
NG_011798.1:g.39550C=
NG_011798.2:g.39658C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2095-53C= MANE Select	ENSP00000497274.1:n.2095-53C=
ENST00000370449.8:c.2095-53C=	ENSP00000359478.4:n.2095-53C=
NM_000392.4:c.2095-53C=	NP_000383.1:n.2095-53C=
XM_006717630.2:c.1399-53C=	XP_006717693.1:n.1399-53C=
XM_006717631.2:c.2095-53C=	XP_006717694.1:n.2095-53C=
XM_011539291.1:c.2095-53C=	XP_011537593.1:n.2095-53C=
XR_945604.1:n.2284-53C=
XR_945605.1:n.2286-53C=
NM_000392.5:c.2095-53C= MANE Select	NP_000383.2:n.2095-53C=
XM_006717630.3:c.1399-53C=	XP_006717693.1:n.1399-53C=
XM_006717631.4:c.2095-53C=	XP_006717694.1:n.2095-53C=
XM_011539291.3:c.2095-53C=	XP_011537593.1:n.2095-53C=
XM_017015675.2:c.2095-53C=	XP_016871164.1:n.2095-53C=
XR_945604.3:n.2338-53C=
XR_945605.3:n.2338-53C=