Canonical Allele Identifier: CA1931496150

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836134C= , CM000672.2:g.99836134C=	GRCh38
NC_000010.10:g.101595891C= , CM000672.1:g.101595891C=	GRCh37
NC_000010.9:g.101585881C=	NCBI36
NG_011798.1:g.58429C=
NG_011798.2:g.58537C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3458C= MANE Select	ENSP00000497274.1:p.Ser1153=
ENST00000370449.8:c.3458C=	ENSP00000359478.4:p.Ser1153=
NM_000392.4:c.3458C=	NP_000383.1:p.Ser1153=
XM_006717630.2:c.2762C=	XP_006717693.1:p.Ser921=
XR_945604.1:n.3647C=
XR_945605.1:n.3649C=
NM_000392.5:c.3458C= MANE Select	NP_000383.2:p.Ser1153=
XM_006717630.3:c.2762C=	XP_006717693.1:p.Ser921=
XR_945604.3:n.3701C=
XR_945605.3:n.3701C=