Canonical Allele Identifier: CA2610497935

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99845853-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845853C>T , CM000672.2:g.99845853C>T	GRCh38
NC_000010.10:g.101605610C>T , CM000672.1:g.101605610C>T	GRCh37
NC_000010.9:g.101595600C>T	NCBI36
NG_011798.1:g.68148C>T
NG_011798.2:g.68256C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4146+71C>T MANE Select	ENSP00000497274.1:n.4146+71C>T
ENST00000648523.1:c.34+71C>T
ENST00000649459.1:n.494+71C>T
ENST00000370449.8:c.4146+71C>T	ENSP00000359478.4:n.4146+71C>T
NM_000392.4:c.4146+71C>T	NP_000383.1:n.4146+71C>T
XM_006717630.2:c.3450+71C>T	XP_006717693.1:n.3450+71C>T
XR_945604.1:n.4276+71C>T
XR_945605.1:n.4210+71C>T
NM_000392.5:c.4146+71C>T MANE Select	NP_000383.2:n.4146+71C>T
XM_006717630.3:c.3450+71C>T	XP_006717693.1:n.3450+71C>T
XR_945604.3:n.4330+71C>T
XR_945605.3:n.4262+71C>T