Canonical Allele Identifier: CA1931513900

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845680C= , CM000672.2:g.99845680C=	GRCh38
NC_000010.10:g.101605437C= , CM000672.1:g.101605437C=	GRCh37
NC_000010.9:g.101595427C=	NCBI36
NG_011798.1:g.67975C=
NG_011798.2:g.68083C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4044C= MANE Select	ENSP00000497274.1:p.Phe1348=
ENST00000649459.1:n.392C=
ENST00000370449.8:c.4044C=	ENSP00000359478.4:p.Phe1348=
NM_000392.4:c.4044C=	NP_000383.1:p.Phe1348=
XM_006717630.2:c.3348C=	XP_006717693.1:p.Phe1116=
XR_945604.1:n.4177-3C=
XR_945605.1:n.4108C=
NM_000392.5:c.4044C= MANE Select	NP_000383.2:p.Phe1348=
XM_006717630.3:c.3348C=	XP_006717693.1:p.Phe1116=
XR_945604.3:n.4231-3C=
XR_945605.3:n.4160C=