Canonical Allele Identifier: CA2739270981

Gene: ABCC2

Linked Data

• ClinVar Variation Id: 2845244
• ClinVar RCV Id: RCV003719421

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836075dup , CM000672.2:g.99836075dup	GRCh38
NC_000010.10:g.101595832dup , CM000672.1:g.101595832dup	GRCh37
NC_000010.9:g.101585822dup	NCBI36
NG_011798.1:g.58370dup
NG_011798.2:g.58478dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-16dup MANE Select	ENSP00000497274.1:n.3415-16dup
ENST00000370449.8:c.3415-16dup	ENSP00000359478.4:n.3415-16dup
NM_000392.4:c.3415-16dup	NP_000383.1:n.3415-16dup
XM_006717630.2:c.2719-16dup	XP_006717693.1:n.2719-16dup
XR_945604.1:n.3604-16dup
XR_945605.1:n.3606-16dup
NM_000392.5:c.3415-16dup MANE Select	NP_000383.2:n.3415-16dup
XM_006717630.3:c.2719-16dup	XP_006717693.1:n.2719-16dup
XR_945604.3:n.3658-16dup
XR_945605.3:n.3658-16dup