Canonical Allele Identifier: CA1680243797
Gene: CCR6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167112513G= , CM000668.2:g.167112513G= GRCh38
NC_000006.11:g.167526001G= , CM000668.1:g.167526001G= GRCh37
NC_000006.10:g.167445991G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609590.2:n.2170-22421G=
ENST00000705249.1:c.1066-23525G= ENSP00000516101.1:n.1066-23525G=
ENST00000705250.1:c.844-23525G= ENSP00000516102.1:n.844-23525G=
ENST00000705251.1:c.*713-23525G= ENSP00000516103.1:n.*713-23525G=
ENST00000705252.1:c.*536-23525G= ENSP00000516104.1:n.*536-23525G=
ENST00000705253.1:c.*536-23525G= ENSP00000516105.1:n.*536-23525G=
ENST00000705254.1:c.673-23525G= ENSP00000516106.1:n.673-23525G=
ENST00000705255.1:n.1692-23525G=
ENST00000400926.5:c.-98+499G= ENSP00000383715.2:n.-98+499G=
NM_004367.5:c.-98+499G= NP_004358.2:n.-98+499G=
XR_943250.1:n.7984C=
XR_943251.1:n.7403C=
XR_001744467.2:n.5919C=
XR_001744469.2:n.5849C=
XR_943250.3:n.7751C=
XR_943251.3:n.7411C=
NM_004367.6:c.-98+499G= NP_004358.2:n.-98+499G=