Canonical Allele Identifier: CA1931511922

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844366C= , CM000672.2:g.99844366C=	GRCh38
NC_000010.10:g.101604123C= , CM000672.1:g.101604123C=	GRCh37
NC_000010.9:g.101594113C=	NCBI36
NG_011798.1:g.66661C=
NG_011798.2:g.66769C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3888C= MANE Select	ENSP00000497274.1:p.Ser1296=
ENST00000649459.1:n.236C=
ENST00000370449.8:c.3888C=	ENSP00000359478.4:p.Ser1296=
NM_000392.4:c.3888C=	NP_000383.1:p.Ser1296=
XM_006717630.2:c.3192C=	XP_006717693.1:p.Ser1064=
XR_945604.1:n.4077C=
XR_945605.1:n.3952C=
NM_000392.5:c.3888C= MANE Select	NP_000383.2:p.Ser1296=
XM_006717630.3:c.3192C=	XP_006717693.1:p.Ser1064=
XR_945604.3:n.4131C=
XR_945605.3:n.4004C=