Canonical Allele Identifier: CA2610497925

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99845837-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845837G>A , CM000672.2:g.99845837G>A	GRCh38
NC_000010.10:g.101605594G>A , CM000672.1:g.101605594G>A	GRCh37
NC_000010.9:g.101595584G>A	NCBI36
NG_011798.1:g.68132G>A
NG_011798.2:g.68240G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4146+55G>A MANE Select	ENSP00000497274.1:n.4146+55G>A
ENST00000648523.1:c.34+55G>A
ENST00000649459.1:n.494+55G>A
ENST00000370449.8:c.4146+55G>A	ENSP00000359478.4:n.4146+55G>A
NM_000392.4:c.4146+55G>A	NP_000383.1:n.4146+55G>A
XM_006717630.2:c.3450+55G>A	XP_006717693.1:n.3450+55G>A
XR_945604.1:n.4276+55G>A
XR_945605.1:n.4210+55G>A
NM_000392.5:c.4146+55G>A MANE Select	NP_000383.2:n.4146+55G>A
XM_006717630.3:c.3450+55G>A	XP_006717693.1:n.3450+55G>A
XR_945604.3:n.4330+55G>A
XR_945605.3:n.4262+55G>A