Canonical Allele Identifier: CA378128093
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99845694C>A , CM000672.2:g.99845694C>A GRCh38
NC_000010.10:g.101605451C>A , CM000672.1:g.101605451C>A GRCh37
NC_000010.9:g.101595441C>A NCBI36
NG_011798.1:g.67989C>A
NG_011798.2:g.68097C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.4058C>A MANE Select ENSP00000497274.1:p.Ala1353Asp
ENST00000649459.1:n.406C>A
ENST00000370449.8:c.4058C>A ENSP00000359478.4:p.Ala1353Asp
NM_000392.4:c.4058C>A NP_000383.1:p.Ala1353Asp
XM_006717630.2:c.3362C>A XP_006717693.1:p.Ala1121Asp
XR_945604.1:n.4188C>A
XR_945605.1:n.4122C>A
NM_000392.5:c.4058C>A MANE Select NP_000383.2:p.Ala1353Asp
XM_006717630.3:c.3362C>A XP_006717693.1:p.Ala1121Asp
XR_945604.3:n.4242C>A
XR_945605.3:n.4174C>A