Canonical Allele Identifier: CA367722741
Gene: CCL26 HGNC NCBI

Linked Data

gnomAD v4: 7-75769700-T-G
MyVariant Identifiers: chr7:g.75399018T>G (hg19) chr7:g.75769700T>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000005180.9:c.278A>C MANE Select ENSP00000005180.4:p.Gln93Pro
ENST00000005180.8:c.278A>C ENSP00000005180.4:p.Gln93Pro
ENST00000394905.2:c.278A>C ENSP00000378365.2:p.Gln93Pro
NM_006072.4:c.278A>C NP_006063.1:p.Gln93Pro
XM_017011671.1:c.440A>C XP_016867160.1:p.Gln147Pro
XM_017011672.1:c.278A>C XP_016867161.1:p.Gln93Pro
NM_001371936.1:c.278A>C NP_001358865.1:p.Gln93Pro
NM_001371938.1:c.278A>C MANE Select NP_001358867.1:p.Gln93Pro
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