Canonical Allele Identifier: CA1931513969

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845704T= , CM000672.2:g.99845704T=	GRCh38
NC_000010.10:g.101605461T= , CM000672.1:g.101605461T=	GRCh37
NC_000010.9:g.101595451T=	NCBI36
NG_011798.1:g.67999T=
NG_011798.2:g.68107T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4068T= MANE Select	ENSP00000497274.1:p.Gly1356=
ENST00000649459.1:n.416T=
ENST00000370449.8:c.4068T=	ENSP00000359478.4:p.Gly1356=
NM_000392.4:c.4068T=	NP_000383.1:p.Gly1356=
XM_006717630.2:c.3372T=	XP_006717693.1:p.Gly1124=
XR_945604.1:n.4198T=
XR_945605.1:n.4132T=
NM_000392.5:c.4068T= MANE Select	NP_000383.2:p.Gly1356=
XM_006717630.3:c.3372T=	XP_006717693.1:p.Gly1124=
XR_945604.3:n.4252T=
XR_945605.3:n.4184T=