Canonical Allele Identifier: CA1931511932

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844370G= , CM000672.2:g.99844370G=	GRCh38
NC_000010.10:g.101604127G= , CM000672.1:g.101604127G=	GRCh37
NC_000010.9:g.101594117G=	NCBI36
NG_011798.1:g.66665G=
NG_011798.2:g.66773G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3892G= MANE Select	ENSP00000497274.1:p.Gly1298=
ENST00000649459.1:n.240G=
ENST00000370449.8:c.3892G=	ENSP00000359478.4:p.Gly1298=
NM_000392.4:c.3892G=	NP_000383.1:p.Gly1298=
XM_006717630.2:c.3196G=	XP_006717693.1:p.Gly1066=
XR_945604.1:n.4081G=
XR_945605.1:n.3956G=
NM_000392.5:c.3892G= MANE Select	NP_000383.2:p.Gly1298=
XM_006717630.3:c.3196G=	XP_006717693.1:p.Gly1066=
XR_945604.3:n.4135G=
XR_945605.3:n.4008G=