Canonical Allele Identifier: CA2681197913

Gene: CCR6

Linked Data

• gnomAD v4: 6-167119423-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119423T>A , CM000668.2:g.167119423T>A	GRCh38
NC_000006.11:g.167532911T>A , CM000668.1:g.167532911T>A	GRCh37
NC_000006.10:g.167452901T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-15511T>A
ENST00000705249.1:c.1066-16615T>A	ENSP00000516101.1:n.1066-16615T>A
ENST00000705250.1:c.844-16615T>A	ENSP00000516102.1:n.844-16615T>A
ENST00000705251.1:c.*713-16615T>A	ENSP00000516103.1:n.*713-16615T>A
ENST00000705252.1:c.*536-16615T>A	ENSP00000516104.1:n.*536-16615T>A
ENST00000705253.1:c.*536-16615T>A	ENSP00000516105.1:n.*536-16615T>A
ENST00000705254.1:c.673-16615T>A	ENSP00000516106.1:n.673-16615T>A
ENST00000705255.1:n.1692-16615T>A
ENST00000400926.5:c.-98+7409T>A	ENSP00000383715.2:n.-98+7409T>A
NM_004367.5:c.-98+7409T>A	NP_004358.2:n.-98+7409T>A
XR_943250.1:n.3172A>T
XR_943251.1:n.3172A>T
XR_001744467.2:n.1188-81A>T
XR_001744469.2:n.1118-81A>T
XR_943250.3:n.2939A>T
XR_943251.3:n.3180A>T
NM_004367.6:c.-98+7409T>A	NP_004358.2:n.-98+7409T>A