Canonical Allele Identifier: CA1931514119

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845767G= , CM000672.2:g.99845767G=	GRCh38
NC_000010.10:g.101605524G= , CM000672.1:g.101605524G=	GRCh37
NC_000010.9:g.101595514G=	NCBI36
NG_011798.1:g.68062G=
NG_011798.2:g.68170G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4131G= MANE Select	ENSP00000497274.1:p.Leu1377=
ENST00000648523.1:c.19G=
ENST00000649459.1:n.479G=
ENST00000370449.8:c.4131G=	ENSP00000359478.4:p.Leu1377=
NM_000392.4:c.4131G=	NP_000383.1:p.Leu1377=
XM_006717630.2:c.3435G=	XP_006717693.1:p.Leu1145=
XR_945604.1:n.4261G=
XR_945605.1:n.4195G=
NM_000392.5:c.4131G= MANE Select	NP_000383.2:p.Leu1377=
XM_006717630.3:c.3435G=	XP_006717693.1:p.Leu1145=
XR_945604.3:n.4315G=
XR_945605.3:n.4247G=