Canonical Allele Identifier: CA1680250595
Gene: CCR6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167119765C= , CM000668.2:g.167119765C= GRCh38
NC_000006.11:g.167533253C= , CM000668.1:g.167533253C= GRCh37
NC_000006.10:g.167453243C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609590.2:n.2170-15169C=
ENST00000705249.1:c.1066-16273C= ENSP00000516101.1:n.1066-16273C=
ENST00000705250.1:c.844-16273C= ENSP00000516102.1:n.844-16273C=
ENST00000705251.1:c.*713-16273C= ENSP00000516103.1:n.*713-16273C=
ENST00000705252.1:c.*536-16273C= ENSP00000516104.1:n.*536-16273C=
ENST00000705253.1:c.*536-16273C= ENSP00000516105.1:n.*536-16273C=
ENST00000705254.1:c.673-16273C= ENSP00000516106.1:n.673-16273C=
ENST00000705255.1:n.1692-16273C=
ENST00000400926.5:c.-98+7751C= ENSP00000383715.2:n.-98+7751C=
NM_004367.5:c.-98+7751C= NP_004358.2:n.-98+7751C=
XR_943250.1:n.2830G=
XR_943251.1:n.2830G=
XR_001744467.2:n.1188-423G=
XR_001744469.2:n.1118-423G=
XR_943250.3:n.2597G=
XR_943251.3:n.2838G=
NM_004367.6:c.-98+7751C= NP_004358.2:n.-98+7751C=