Canonical Allele Identifier: CA2681199653
Gene: CCR6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167127344T>C , CM000668.2:g.167127344T>C GRCh38
NC_000006.11:g.167540832T>C , CM000668.1:g.167540832T>C GRCh37
NC_000006.10:g.167460822T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609590.2:n.2170-7590T>C
ENST00000705249.1:c.1066-8694T>C ENSP00000516101.1:n.1066-8694T>C
ENST00000705250.1:c.844-8694T>C ENSP00000516102.1:n.844-8694T>C
ENST00000705251.1:c.*713-8694T>C ENSP00000516103.1:n.*713-8694T>C
ENST00000705252.1:c.*536-8694T>C ENSP00000516104.1:n.*536-8694T>C
ENST00000705253.1:c.*536-8694T>C ENSP00000516105.1:n.*536-8694T>C
ENST00000705254.1:c.673-8694T>C ENSP00000516106.1:n.673-8694T>C
ENST00000705255.1:n.1692-8694T>C
ENST00000341935.10:c.-98+4121T>C MANE Select ENSP00000343952.5:n.-98+4121T>C
ENST00000643861.1:c.-98+4121T>C ENSP00000493637.1:n.-98+4121T>C
ENST00000341935.9:c.-98+4121T>C ENSP00000343952.5:n.-98+4121T>C
ENST00000349984.6:c.-98+4121T>C ENSP00000339393.4:n.-98+4121T>C
ENST00000400926.5:c.-97-8694T>C ENSP00000383715.2:n.-97-8694T>C
NM_004367.5:c.-97-8694T>C NP_004358.2:n.-97-8694T>C
NM_031409.3:c.-98+4121T>C NP_113597.2:n.-98+4121T>C
XR_001744470.1:n.1277A>G
NM_004367.6:c.-97-8694T>C NP_004358.2:n.-97-8694T>C
NM_031409.4:c.-98+4121T>C MANE Select NP_113597.2:n.-98+4121T>C
NM_001394582.1:c.-98+4121T>C NP_001381511.1:n.-98+4121T>C