Canonical Allele Identifier: CA1931496080

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836112C= , CM000672.2:g.99836112C=	GRCh38
NC_000010.10:g.101595869C= , CM000672.1:g.101595869C=	GRCh37
NC_000010.9:g.101585859C=	NCBI36
NG_011798.1:g.58407C=
NG_011798.2:g.58515C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3436C= MANE Select	ENSP00000497274.1:p.Arg1146=
ENST00000370449.8:c.3436C=	ENSP00000359478.4:p.Arg1146=
NM_000392.4:c.3436C=	NP_000383.1:p.Arg1146=
XM_006717630.2:c.2740C=	XP_006717693.1:p.Arg914=
XR_945604.1:n.3625C=
XR_945605.1:n.3627C=
NM_000392.5:c.3436C= MANE Select	NP_000383.2:p.Arg1146=
XM_006717630.3:c.2740C=	XP_006717693.1:p.Arg914=
XR_945604.3:n.3679C=
XR_945605.3:n.3679C=