Canonical Allele Identifier: CA5644023
Gene: ABCC2 HGNC NCBI

Linked Data

dbSNP Id: rs780578539

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4054G>A MANE Select ENSP00000497274.1:p.Glu1352Lys
ENST00000649459.1:n.402G>A
ENST00000370449.8:c.4054G>A ENSP00000359478.4:p.Glu1352Lys
NM_000392.4:c.4054G>A NP_000383.1:p.Glu1352Lys
XM_006717630.2:c.3358G>A XP_006717693.1:p.Glu1120Lys
XR_945604.1:n.4184G>A
XR_945605.1:n.4118G>A
NM_000392.5:c.4054G>A MANE Select NP_000383.2:p.Glu1352Lys
XM_006717630.3:c.3358G>A XP_006717693.1:p.Glu1120Lys
XR_945604.3:n.4238G>A
XR_945605.3:n.4170G>A