Canonical Allele Identifier: CA1931489255

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830417C= , CM000672.2:g.99830417C=	GRCh38
NC_000010.10:g.101590174C= , CM000672.1:g.101590174C=	GRCh37
NC_000010.9:g.101580164C=	NCBI36
NG_011798.1:g.52712C=
NG_011798.2:g.52820C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2731C= MANE Select	ENSP00000497274.1:p.Arg911=
ENST00000370449.8:c.2731C=	ENSP00000359478.4:p.Arg911=
NM_000392.4:c.2731C=	NP_000383.1:p.Arg911=
XM_006717630.2:c.2035C=	XP_006717693.1:p.Arg679=
XM_011539291.1:c.2731C=	XP_011537593.1:p.Arg911=
XR_945604.1:n.2920C=
XR_945605.1:n.2922C=
NM_000392.5:c.2731C= MANE Select	NP_000383.2:p.Arg911=
XM_006717630.3:c.2035C=	XP_006717693.1:p.Arg679=
XM_011539291.3:c.2731C=	XP_011537593.1:p.Arg911=
XR_945604.3:n.2974C=
XR_945605.3:n.2974C=