Canonical Allele Identifier: CA1931496460

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836263_99836264delinsGT , CM000672.2:g.99836263_99836264delinsGT	GRCh38
NC_000010.10:g.101596020_101596021delinsGT , CM000672.1:g.101596020_101596021delinsGT	GRCh37
NC_000010.9:g.101586010_101586011delinsGT	NCBI36
NG_011798.1:g.58558_58559delinsGT
NG_011798.2:g.58666_58667delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3587_3588delinsGT MANE Select	ENSP00000497274.1:p.Cys1196=
ENST00000370449.8:c.3587_3588delinsGT	ENSP00000359478.4:p.Cys1196=
NM_000392.4:c.3587_3588delinsGT	NP_000383.1:p.Cys1196=
XM_006717630.2:c.2891_2892delinsGT	XP_006717693.1:p.Cys964=
XR_945604.1:n.3776_3777delinsGT
XR_945605.1:n.3778_3779delinsGT
NM_000392.5:c.3587_3588delinsGT MANE Select	NP_000383.2:p.Cys1196=
XM_006717630.3:c.2891_2892delinsGT	XP_006717693.1:p.Cys964=
XR_945604.3:n.3830_3831delinsGT
XR_945605.3:n.3830_3831delinsGT