Canonical Allele Identifier: CA1931496312

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836205G= , CM000672.2:g.99836205G=	GRCh38
NC_000010.10:g.101595962G= , CM000672.1:g.101595962G=	GRCh37
NC_000010.9:g.101585952G=	NCBI36
NG_011798.1:g.58500G=
NG_011798.2:g.58608G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3529G= MANE Select	ENSP00000497274.1:p.Glu1177=
ENST00000370449.8:c.3529G=	ENSP00000359478.4:p.Glu1177=
NM_000392.4:c.3529G=	NP_000383.1:p.Glu1177=
XM_006717630.2:c.2833G=	XP_006717693.1:p.Glu945=
XR_945604.1:n.3718G=
XR_945605.1:n.3720G=
NM_000392.5:c.3529G= MANE Select	NP_000383.2:p.Glu1177=
XM_006717630.3:c.2833G=	XP_006717693.1:p.Glu945=
XR_945604.3:n.3772G=
XR_945605.3:n.3772G=