Canonical Allele Identifier: CA918744468

Gene: ABCC2

Linked Data

• dbSNP Id: rs1564701873

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845913_99845914insCGGGATACTCG , CM000672.2:g.99845913_99845914insCGGGATACTCG	GRCh38
NC_000010.10:g.101605670_101605671insCGGGATACTCG , CM000672.1:g.101605670_101605671insCGGGATACTCG	GRCh37
NC_000010.9:g.101595660_101595661insCGGGATACTCG	NCBI36
NG_011798.1:g.68208_68209insCGGGATACTCG
NG_011798.2:g.68316_68317insCGGGATACTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4146+131_4146+132insCGGGATACTCG MANE Select	ENSP00000497274.1:n.4146+131_4146+132insCGGGATACTCG
ENST00000648523.1:c.34+131_34+132insCGGGATACTCG
ENST00000649459.1:n.494+131_494+132insCGGGATACTCG
ENST00000370449.8:c.4146+131_4146+132insCGGGATACTCG	ENSP00000359478.4:n.4146+131_4146+132insCGGGATACTCG
NM_000392.4:c.4146+131_4146+132insCGGGATACTCG	NP_000383.1:n.4146+131_4146+132insCGGGATACTCG
XM_006717630.2:c.3450+131_3450+132insCGGGATACTCG	XP_006717693.1:n.3450+131_3450+132insCGGGATACTCG
XR_945604.1:n.4276+131_4276+132insCGGGATACTCG
XR_945605.1:n.4210+131_4210+132insCGGGATACTCG
NM_000392.5:c.4146+131_4146+132insCGGGATACTCG MANE Select	NP_000383.2:n.4146+131_4146+132insCGGGATACTCG
XM_006717630.3:c.3450+131_3450+132insCGGGATACTCG	XP_006717693.1:n.3450+131_3450+132insCGGGATACTCG
XR_945604.3:n.4330+131_4330+132insCGGGATACTCG
XR_945605.3:n.4262+131_4262+132insCGGGATACTCG