Canonical Allele Identifier: CA1931496459

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836263G= , CM000672.2:g.99836263G=	GRCh38
NC_000010.10:g.101596020G= , CM000672.1:g.101596020G=	GRCh37
NC_000010.9:g.101586010G=	NCBI36
NG_011798.1:g.58558G=
NG_011798.2:g.58666G=

Transcript Alleles

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