Canonical Allele Identifier: CA2610497982

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99845914-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845914A>G , CM000672.2:g.99845914A>G	GRCh38
NC_000010.10:g.101605671A>G , CM000672.1:g.101605671A>G	GRCh37
NC_000010.9:g.101595661A>G	NCBI36
NG_011798.1:g.68209A>G
NG_011798.2:g.68317A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4146+132A>G MANE Select	ENSP00000497274.1:n.4146+132A>G
ENST00000648523.1:c.34+132A>G
ENST00000649459.1:n.494+132A>G
ENST00000370449.8:c.4146+132A>G	ENSP00000359478.4:n.4146+132A>G
NM_000392.4:c.4146+132A>G	NP_000383.1:n.4146+132A>G
XM_006717630.2:c.3450+132A>G	XP_006717693.1:n.3450+132A>G
XR_945604.1:n.4276+132A>G
XR_945605.1:n.4210+132A>G
NM_000392.5:c.4146+132A>G MANE Select	NP_000383.2:n.4146+132A>G
XM_006717630.3:c.3450+132A>G	XP_006717693.1:n.3450+132A>G
XR_945604.3:n.4330+132A>G
XR_945605.3:n.4262+132A>G