Canonical Allele Identifier: CA1931513833

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845655A= , CM000672.2:g.99845655A=	GRCh38
NC_000010.10:g.101605412A= , CM000672.1:g.101605412A=	GRCh37
NC_000010.9:g.101595402A=	NCBI36
NG_011798.1:g.67950A=
NG_011798.2:g.68058A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4019A= MANE Select	ENSP00000497274.1:p.Lys1340=
ENST00000649459.1:n.367A=
ENST00000370449.8:c.4019A=	ENSP00000359478.4:p.Lys1340=
NM_000392.4:c.4019A=	NP_000383.1:p.Lys1340=
XM_006717630.2:c.3323A=	XP_006717693.1:p.Lys1108=
XR_945604.1:n.4177-28A=
XR_945605.1:n.4083A=
NM_000392.5:c.4019A= MANE Select	NP_000383.2:p.Lys1340=
XM_006717630.3:c.3323A=	XP_006717693.1:p.Lys1108=
XR_945604.3:n.4231-28A=
XR_945605.3:n.4135A=