Canonical Allele Identifier: CA1931496090

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836116A= , CM000672.2:g.99836116A=	GRCh38
NC_000010.10:g.101595873A= , CM000672.1:g.101595873A=	GRCh37
NC_000010.9:g.101585863A=	NCBI36
NG_011798.1:g.58411A=
NG_011798.2:g.58519A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3440A= MANE Select	ENSP00000497274.1:p.Gln1147=
ENST00000370449.8:c.3440A=	ENSP00000359478.4:p.Gln1147=
NM_000392.4:c.3440A=	NP_000383.1:p.Gln1147=
XM_006717630.2:c.2744A=	XP_006717693.1:p.Gln915=
XR_945604.1:n.3629A=
XR_945605.1:n.3631A=
NM_000392.5:c.3440A= MANE Select	NP_000383.2:p.Gln1147=
XM_006717630.3:c.2744A=	XP_006717693.1:p.Gln915=
XR_945604.3:n.3683A=
XR_945605.3:n.3683A=