Canonical Allele Identifier: CA2681197541
Gene: CCR6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167119113C>A , CM000668.2:g.167119113C>A GRCh38
NC_000006.11:g.167532601C>A , CM000668.1:g.167532601C>A GRCh37
NC_000006.10:g.167452591C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609590.2:n.2170-15821C>A
ENST00000705249.1:c.1066-16925C>A ENSP00000516101.1:n.1066-16925C>A
ENST00000705250.1:c.844-16925C>A ENSP00000516102.1:n.844-16925C>A
ENST00000705251.1:c.*713-16925C>A ENSP00000516103.1:n.*713-16925C>A
ENST00000705252.1:c.*536-16925C>A ENSP00000516104.1:n.*536-16925C>A
ENST00000705253.1:c.*536-16925C>A ENSP00000516105.1:n.*536-16925C>A
ENST00000705254.1:c.673-16925C>A ENSP00000516106.1:n.673-16925C>A
ENST00000705255.1:n.1692-16925C>A
ENST00000400926.5:c.-98+7099C>A ENSP00000383715.2:n.-98+7099C>A
NM_004367.5:c.-98+7099C>A NP_004358.2:n.-98+7099C>A
XR_943250.1:n.3409+73G>T
XR_943251.1:n.3409+73G>T
XR_001744467.2:n.1344+73G>T
XR_001744469.2:n.1274+73G>T
XR_943250.3:n.3176+73G>T
XR_943251.3:n.3417+73G>T
NM_004367.6:c.-98+7099C>A NP_004358.2:n.-98+7099C>A