Canonical Allele Identifier: CA1931496136

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836131A= , CM000672.2:g.99836131A=	GRCh38
NC_000010.10:g.101595888A= , CM000672.1:g.101595888A=	GRCh37
NC_000010.9:g.101585878A=	NCBI36
NG_011798.1:g.58426A=
NG_011798.2:g.58534A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3455A= MANE Select	ENSP00000497274.1:p.Asp1152=
ENST00000370449.8:c.3455A=	ENSP00000359478.4:p.Asp1152=
NM_000392.4:c.3455A=	NP_000383.1:p.Asp1152=
XM_006717630.2:c.2759A=	XP_006717693.1:p.Asp920=
XR_945604.1:n.3644A=
XR_945605.1:n.3646A=
NM_000392.5:c.3455A= MANE Select	NP_000383.2:p.Asp1152=
XM_006717630.3:c.2759A=	XP_006717693.1:p.Asp920=
XR_945604.3:n.3698A=
XR_945605.3:n.3698A=