Canonical Allele Identifier: CA1680250443
Gene: CCR6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167119607A= , CM000668.2:g.167119607A= GRCh38
NC_000006.11:g.167533095A= , CM000668.1:g.167533095A= GRCh37
NC_000006.10:g.167453085A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609590.2:n.2170-15327A=
ENST00000705249.1:c.1066-16431A= ENSP00000516101.1:n.1066-16431A=
ENST00000705250.1:c.844-16431A= ENSP00000516102.1:n.844-16431A=
ENST00000705251.1:c.*713-16431A= ENSP00000516103.1:n.*713-16431A=
ENST00000705252.1:c.*536-16431A= ENSP00000516104.1:n.*536-16431A=
ENST00000705253.1:c.*536-16431A= ENSP00000516105.1:n.*536-16431A=
ENST00000705254.1:c.673-16431A= ENSP00000516106.1:n.673-16431A=
ENST00000705255.1:n.1692-16431A=
ENST00000400926.5:c.-98+7593A= ENSP00000383715.2:n.-98+7593A=
NM_004367.5:c.-98+7593A= NP_004358.2:n.-98+7593A=
XR_943250.1:n.2988T=
XR_943251.1:n.2988T=
XR_001744467.2:n.1188-265T=
XR_001744469.2:n.1118-265T=
XR_943250.3:n.2755T=
XR_943251.3:n.2996T=
NM_004367.6:c.-98+7593A= NP_004358.2:n.-98+7593A=