Canonical Allele Identifier: CA1931496132

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836130G= , CM000672.2:g.99836130G=	GRCh38
NC_000010.10:g.101595887G= , CM000672.1:g.101595887G=	GRCh37
NC_000010.9:g.101585877G=	NCBI36
NG_011798.1:g.58425G=
NG_011798.2:g.58533G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3454G= MANE Select	ENSP00000497274.1:p.Asp1152=
ENST00000370449.8:c.3454G=	ENSP00000359478.4:p.Asp1152=
NM_000392.4:c.3454G=	NP_000383.1:p.Asp1152=
XM_006717630.2:c.2758G=	XP_006717693.1:p.Asp920=
XR_945604.1:n.3643G=
XR_945605.1:n.3645G=
NM_000392.5:c.3454G= MANE Select	NP_000383.2:p.Asp1152=
XM_006717630.3:c.2758G=	XP_006717693.1:p.Asp920=
XR_945604.3:n.3697G=
XR_945605.3:n.3697G=