Canonical Allele Identifier: CA1931514401

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845892G= , CM000672.2:g.99845892G=	GRCh38
NC_000010.10:g.101605649G= , CM000672.1:g.101605649G=	GRCh37
NC_000010.9:g.101595639G=	NCBI36
NG_011798.1:g.68187G=
NG_011798.2:g.68295G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4146+110G= MANE Select	ENSP00000497274.1:n.4146+110G=
ENST00000648523.1:c.34+110G=
ENST00000649459.1:n.494+110G=
ENST00000370449.8:c.4146+110G=	ENSP00000359478.4:n.4146+110G=
NM_000392.4:c.4146+110G=	NP_000383.1:n.4146+110G=
XM_006717630.2:c.3450+110G=	XP_006717693.1:n.3450+110G=
XR_945604.1:n.4276+110G=
XR_945605.1:n.4210+110G=
NM_000392.5:c.4146+110G= MANE Select	NP_000383.2:n.4146+110G=
XM_006717630.3:c.3450+110G=	XP_006717693.1:n.3450+110G=
XR_945604.3:n.4330+110G=
XR_945605.3:n.4262+110G=