Canonical Allele Identifier: CA1931514374

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845877A= , CM000672.2:g.99845877A=	GRCh38
NC_000010.10:g.101605634A= , CM000672.1:g.101605634A=	GRCh37
NC_000010.9:g.101595624A=	NCBI36
NG_011798.1:g.68172A=
NG_011798.2:g.68280A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4146+95A= MANE Select	ENSP00000497274.1:n.4146+95A=
ENST00000648523.1:c.34+95A=
ENST00000649459.1:n.494+95A=
ENST00000370449.8:c.4146+95A=	ENSP00000359478.4:n.4146+95A=
NM_000392.4:c.4146+95A=	NP_000383.1:n.4146+95A=
XM_006717630.2:c.3450+95A=	XP_006717693.1:n.3450+95A=
XR_945604.1:n.4276+95A=
XR_945605.1:n.4210+95A=
NM_000392.5:c.4146+95A= MANE Select	NP_000383.2:n.4146+95A=
XM_006717630.3:c.3450+95A=	XP_006717693.1:n.3450+95A=
XR_945604.3:n.4330+95A=
XR_945605.3:n.4262+95A=