Canonical Allele Identifier: CA1680250575
Gene: CCR6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167119732T= , CM000668.2:g.167119732T= GRCh38
NC_000006.11:g.167533220T= , CM000668.1:g.167533220T= GRCh37
NC_000006.10:g.167453210T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609590.2:n.2170-15202T=
ENST00000705249.1:c.1066-16306T= ENSP00000516101.1:n.1066-16306T=
ENST00000705250.1:c.844-16306T= ENSP00000516102.1:n.844-16306T=
ENST00000705251.1:c.*713-16306T= ENSP00000516103.1:n.*713-16306T=
ENST00000705252.1:c.*536-16306T= ENSP00000516104.1:n.*536-16306T=
ENST00000705253.1:c.*536-16306T= ENSP00000516105.1:n.*536-16306T=
ENST00000705254.1:c.673-16306T= ENSP00000516106.1:n.673-16306T=
ENST00000705255.1:n.1692-16306T=
ENST00000400926.5:c.-98+7718T= ENSP00000383715.2:n.-98+7718T=
NM_004367.5:c.-98+7718T= NP_004358.2:n.-98+7718T=
XR_943250.1:n.2863A=
XR_943251.1:n.2863A=
XR_001744467.2:n.1188-390A=
XR_001744469.2:n.1118-390A=
XR_943250.3:n.2630A=
XR_943251.3:n.2871A=
NM_004367.6:c.-98+7718T= NP_004358.2:n.-98+7718T=