Canonical Allele Identifier: CA378126699
Gene: ABCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99844353C>A , CM000672.2:g.99844353C>A GRCh38
NC_000010.10:g.101604110C>A , CM000672.1:g.101604110C>A GRCh37
NC_000010.9:g.101594100C>A NCBI36
NG_011798.1:g.66648C>A
NG_011798.2:g.66756C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647814.1:c.3875C>A MANE Select ENSP00000497274.1:p.Pro1292Gln
ENST00000649459.1:n.223C>A
ENST00000370449.8:c.3875C>A ENSP00000359478.4:p.Pro1292Gln
NM_000392.4:c.3875C>A NP_000383.1:p.Pro1292Gln
XM_006717630.2:c.3179C>A XP_006717693.1:p.Pro1060Gln
XR_945604.1:n.4064C>A
XR_945605.1:n.3939C>A
NM_000392.5:c.3875C>A MANE Select NP_000383.2:p.Pro1292Gln
XM_006717630.3:c.3179C>A XP_006717693.1:p.Pro1060Gln
XR_945604.3:n.4118C>A
XR_945605.3:n.3991C>A