Canonical Allele Identifier: CA1931513930
Gene: ABCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845690G= , CM000672.2:g.99845690G= GRCh38
NC_000010.10:g.101605447G= , CM000672.1:g.101605447G= GRCh37
NC_000010.9:g.101595437G= NCBI36
NG_011798.1:g.67985G=
NG_011798.2:g.68093G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4054G= MANE Select ENSP00000497274.1:p.Glu1352=
ENST00000649459.1:n.402G=
ENST00000370449.8:c.4054G= ENSP00000359478.4:p.Glu1352=
NM_000392.4:c.4054G= NP_000383.1:p.Glu1352=
XM_006717630.2:c.3358G= XP_006717693.1:p.Glu1120=
XR_945604.1:n.4184G=
XR_945605.1:n.4118G=
NM_000392.5:c.4054G= MANE Select NP_000383.2:p.Glu1352=
XM_006717630.3:c.3358G= XP_006717693.1:p.Glu1120=
XR_945604.3:n.4238G=
XR_945605.3:n.4170G=