Canonical Allele Identifier: CA1931513829

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845649C= , CM000672.2:g.99845649C=	GRCh38
NC_000010.10:g.101605406C= , CM000672.1:g.101605406C=	GRCh37
NC_000010.9:g.101595396C=	NCBI36
NG_011798.1:g.67944C=
NG_011798.2:g.68052C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4013C= MANE Select	ENSP00000497274.1:p.Ala1338=
ENST00000649459.1:n.361C=
ENST00000370449.8:c.4013C=	ENSP00000359478.4:p.Ala1338=
NM_000392.4:c.4013C=	NP_000383.1:p.Ala1338=
XM_006717630.2:c.3317C=	XP_006717693.1:p.Ala1106=
XR_945604.1:n.4177-34C=
XR_945605.1:n.4077C=
NM_000392.5:c.4013C= MANE Select	NP_000383.2:p.Ala1338=
XM_006717630.3:c.3317C=	XP_006717693.1:p.Ala1106=
XR_945604.3:n.4231-34C=
XR_945605.3:n.4129C=