Canonical Allele Identifier: CA2789199793

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845586_99845589del , CM000672.2:g.99845586_99845589del	GRCh38
NC_000010.10:g.101605343_101605346del , CM000672.1:g.101605343_101605346del	GRCh37
NC_000010.9:g.101595333_101595336del	NCBI36
NG_011798.1:g.67881_67884del
NG_011798.2:g.67989_67992del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3988-38_3988-35del MANE Select	ENSP00000497274.1:n.3988-38_3988-35del
ENST00000649459.1:n.336-38_336-35del
ENST00000370449.8:c.3988-38_3988-35del	ENSP00000359478.4:n.3988-38_3988-35del
NM_000392.4:c.3988-38_3988-35del	NP_000383.1:n.3988-38_3988-35del
XM_006717630.2:c.3292-38_3292-35del	XP_006717693.1:n.3292-38_3292-35del
XR_945604.1:n.4177-97_4177-94del
XR_945605.1:n.4052-38_4052-35del
NM_000392.5:c.3988-38_3988-35del MANE Select	NP_000383.2:n.3988-38_3988-35del
XM_006717630.3:c.3292-38_3292-35del	XP_006717693.1:n.3292-38_3292-35del
XR_945604.3:n.4231-97_4231-94del
XR_945605.3:n.4104-38_4104-35del