Canonical Allele Identifier: CA2722458918

Gene: ABCC2

Linked Data

• dbSNP Id: rs2133149909

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845910A>T , CM000672.2:g.99845910A>T	GRCh38
NC_000010.10:g.101605667A>T , CM000672.1:g.101605667A>T	GRCh37
NC_000010.9:g.101595657A>T	NCBI36
NG_011798.1:g.68205A>T
NG_011798.2:g.68313A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4146+128A>T MANE Select	ENSP00000497274.1:n.4146+128A>T
ENST00000648523.1:c.34+128A>T
ENST00000649459.1:n.494+128A>T
ENST00000370449.8:c.4146+128A>T	ENSP00000359478.4:n.4146+128A>T
NM_000392.4:c.4146+128A>T	NP_000383.1:n.4146+128A>T
XM_006717630.2:c.3450+128A>T	XP_006717693.1:n.3450+128A>T
XR_945604.1:n.4276+128A>T
XR_945605.1:n.4210+128A>T
NM_000392.5:c.4146+128A>T MANE Select	NP_000383.2:n.4146+128A>T
XM_006717630.3:c.3450+128A>T	XP_006717693.1:n.3450+128A>T
XR_945604.3:n.4330+128A>T
XR_945605.3:n.4262+128A>T