Canonical Allele Identifier: CA2610495296

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99818692-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99818692C>A , CM000672.2:g.99818692C>A	GRCh38
NC_000010.10:g.101578449C>A , CM000672.1:g.101578449C>A	GRCh37
NC_000010.9:g.101568439C>A	NCBI36
NG_011798.1:g.40987C>A
NG_011798.2:g.41095C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2272-98C>A MANE Select	ENSP00000497274.1:n.2272-98C>A
ENST00000370449.8:c.2272-98C>A	ENSP00000359478.4:n.2272-98C>A
NM_000392.4:c.2272-98C>A	NP_000383.1:n.2272-98C>A
XM_006717630.2:c.1576-98C>A	XP_006717693.1:n.1576-98C>A
XM_006717631.2:c.2272-98C>A	XP_006717694.1:n.2272-98C>A
XM_011539291.1:c.2272-98C>A	XP_011537593.1:n.2272-98C>A
XR_945604.1:n.2461-98C>A
XR_945605.1:n.2463-98C>A
NM_000392.5:c.2272-98C>A MANE Select	NP_000383.2:n.2272-98C>A
XM_006717630.3:c.1576-98C>A	XP_006717693.1:n.1576-98C>A
XM_006717631.4:c.2272-98C>A	XP_006717694.1:n.2272-98C>A
XM_011539291.3:c.2272-98C>A	XP_011537593.1:n.2272-98C>A
XM_017015675.2:c.2272-98C>A	XP_016871164.1:n.2272-98C>A
XR_945604.3:n.2515-98C>A
XR_945605.3:n.2515-98C>A