Canonical Allele Identifier: CA2610497937

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99845858-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845859del , CM000672.2:g.99845859del	GRCh38
NC_000010.10:g.101605616del , CM000672.1:g.101605616del	GRCh37
NC_000010.9:g.101595606del	NCBI36
NG_011798.1:g.68154del
NG_011798.2:g.68262del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4146+77del MANE Select	ENSP00000497274.1:n.4146+77del
ENST00000648523.1:c.34+77del
ENST00000649459.1:n.494+77del
ENST00000370449.8:c.4146+77del	ENSP00000359478.4:n.4146+77del
NM_000392.4:c.4146+77del	NP_000383.1:n.4146+77del
XM_006717630.2:c.3450+77del	XP_006717693.1:n.3450+77del
XR_945604.1:n.4276+77del
XR_945605.1:n.4210+77del
NM_000392.5:c.4146+77del MANE Select	NP_000383.2:n.4146+77del
XM_006717630.3:c.3450+77del	XP_006717693.1:n.3450+77del
XR_945604.3:n.4330+77del
XR_945605.3:n.4262+77del