Canonical Allele Identifier: CA2722455093

Gene: ABCC2

Linked Data

• dbSNP Id: rs2133159597

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99851388_99851392del , CM000672.2:g.99851388_99851392del	GRCh38
NC_000010.10:g.101611145_101611149del , CM000672.1:g.101611145_101611149del	GRCh37
NC_000010.9:g.101601135_101601139del	NCBI36
NG_011798.1:g.73683_73687del
NG_011798.2:g.73791_73795del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4509-114_4509-110del MANE Select	ENSP00000497274.1:n.4509-114_4509-110del
ENST00000648523.1:c.579-114_579-110del
ENST00000370449.8:c.4509-114_4509-110del	ENSP00000359478.4:n.4509-114_4509-110del
NM_000392.4:c.4509-114_4509-110del	NP_000383.1:n.4509-114_4509-110del
XM_006717630.2:c.3813-114_3813-110del	XP_006717693.1:n.3813-114_3813-110del
XR_945605.1:n.4573-114_4573-110del
NM_000392.5:c.4509-114_4509-110del MANE Select	NP_000383.2:n.4509-114_4509-110del
XM_006717630.3:c.3813-114_3813-110del	XP_006717693.1:n.3813-114_3813-110del
XR_945605.3:n.4625-114_4625-110del