Canonical Allele Identifier: CA4302804
Gene: CCL26 HGNC NCBI

Linked Data

dbSNP Id: rs782148218
gnomAD v2: 7-75399026-A-C
gnomAD v4: 7-75769708-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.75769708A>C , CM000669.2:g.75769708A>C GRCh38
NC_000007.13:g.75399026A>C , CM000669.1:g.75399026A>C GRCh37
NC_000007.12:g.75236962A>C NCBI36
NG_015989.1:g.25039T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000005180.9:c.270T>G MANE Select ENSP00000005180.4:p.Thr90=
ENST00000005180.8:c.270T>G ENSP00000005180.4:p.Thr90=
ENST00000394905.2:c.270T>G ENSP00000378365.2:p.Thr90=
NM_006072.4:c.270T>G NP_006063.1:p.Thr90=
XM_017011671.1:c.432T>G XP_016867160.1:p.Thr144=
XM_017011672.1:c.270T>G XP_016867161.1:p.Thr90=
NM_001371936.1:c.270T>G NP_001358865.1:p.Thr90=
NM_001371938.1:c.270T>G MANE Select NP_001358867.1:p.Thr90=