Canonical Allele Identifier: CA367722739
Gene: CCL26 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75769700T>C , CM000669.2:g.75769700T>C GRCh38
NC_000007.13:g.75399018T>C , CM000669.1:g.75399018T>C GRCh37
NC_000007.12:g.75236954T>C NCBI36
NG_015989.1:g.25047A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000005180.9:c.278A>G MANE Select ENSP00000005180.4:p.Gln93Arg
ENST00000005180.8:c.278A>G ENSP00000005180.4:p.Gln93Arg
ENST00000394905.2:c.278A>G ENSP00000378365.2:p.Gln93Arg
NM_006072.4:c.278A>G NP_006063.1:p.Gln93Arg
XM_017011671.1:c.440A>G XP_016867160.1:p.Gln147Arg
XM_017011672.1:c.278A>G XP_016867161.1:p.Gln93Arg
NM_001371936.1:c.278A>G NP_001358865.1:p.Gln93Arg
NM_001371938.1:c.278A>G MANE Select NP_001358867.1:p.Gln93Arg