Canonical Allele Identifier: CA1931514417

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845906C= , CM000672.2:g.99845906C=	GRCh38
NC_000010.10:g.101605663C= , CM000672.1:g.101605663C=	GRCh37
NC_000010.9:g.101595653C=	NCBI36
NG_011798.1:g.68201C=
NG_011798.2:g.68309C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4146+124C= MANE Select	ENSP00000497274.1:n.4146+124C=
ENST00000648523.1:c.34+124C=
ENST00000649459.1:n.494+124C=
ENST00000370449.8:c.4146+124C=	ENSP00000359478.4:n.4146+124C=
NM_000392.4:c.4146+124C=	NP_000383.1:n.4146+124C=
XM_006717630.2:c.3450+124C=	XP_006717693.1:n.3450+124C=
XR_945604.1:n.4276+124C=
XR_945605.1:n.4210+124C=
NM_000392.5:c.4146+124C= MANE Select	NP_000383.2:n.4146+124C=
XM_006717630.3:c.3450+124C=	XP_006717693.1:n.3450+124C=
XR_945604.3:n.4330+124C=
XR_945605.3:n.4262+124C=