Canonical Allele Identifier: CA378128086
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845693G>A , CM000672.2:g.99845693G>A GRCh38
NC_000010.10:g.101605450G>A , CM000672.1:g.101605450G>A GRCh37
NC_000010.9:g.101595440G>A NCBI36
NG_011798.1:g.67988G>A
NG_011798.2:g.68096G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4057G>A MANE Select ENSP00000497274.1:p.Ala1353Thr
ENST00000649459.1:n.405G>A
ENST00000370449.8:c.4057G>A ENSP00000359478.4:p.Ala1353Thr
NM_000392.4:c.4057G>A NP_000383.1:p.Ala1353Thr
XM_006717630.2:c.3361G>A XP_006717693.1:p.Ala1121Thr
XR_945604.1:n.4187G>A
XR_945605.1:n.4121G>A
NM_000392.5:c.4057G>A MANE Select NP_000383.2:p.Ala1353Thr
XM_006717630.3:c.3361G>A XP_006717693.1:p.Ala1121Thr
XR_945604.3:n.4241G>A
XR_945605.3:n.4173G>A