Canonical Allele Identifier: CA212872805

Gene: ABCC2

Linked Data

• dbSNP Id: rs35296652

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99851352dup , CM000672.2:g.99851352dup	GRCh38
NC_000010.10:g.101611109dup , CM000672.1:g.101611109dup	GRCh37
NC_000010.9:g.101601099dup	NCBI36
NG_011798.1:g.73647dup
NG_011798.2:g.73755dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4509-150dup MANE Select	ENSP00000497274.1:n.4509-150dup
ENST00000648523.1:c.579-150dup
ENST00000370449.8:c.4509-150dup	ENSP00000359478.4:n.4509-150dup
NM_000392.4:c.4509-150dup	NP_000383.1:n.4509-150dup
XM_006717630.2:c.3813-150dup	XP_006717693.1:n.3813-150dup
XR_945605.1:n.4573-150dup
NM_000392.5:c.4509-150dup MANE Select	NP_000383.2:n.4509-150dup
XM_006717630.3:c.3813-150dup	XP_006717693.1:n.3813-150dup
XR_945605.3:n.4625-150dup