Canonical Allele Identifier: CA151949804

Gene: CCR6

Linked Data

• dbSNP Id: rs532276906
• gnomAD v3: 6-167119654-G-A
• gnomAD v4: 6-167119654-G-A
• MyVariant Identifiers: chr6:g.167533142G>A (hg19) ; chr6:g.167119654G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119654G>A , CM000668.2:g.167119654G>A	GRCh38
NC_000006.11:g.167533142G>A , CM000668.1:g.167533142G>A	GRCh37
NC_000006.10:g.167453132G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-15280G>A
ENST00000705249.1:c.1066-16384G>A	ENSP00000516101.1:n.1066-16384G>A
ENST00000705250.1:c.844-16384G>A	ENSP00000516102.1:n.844-16384G>A
ENST00000705251.1:c.*713-16384G>A	ENSP00000516103.1:n.*713-16384G>A
ENST00000705252.1:c.*536-16384G>A	ENSP00000516104.1:n.*536-16384G>A
ENST00000705253.1:c.*536-16384G>A	ENSP00000516105.1:n.*536-16384G>A
ENST00000705254.1:c.673-16384G>A	ENSP00000516106.1:n.673-16384G>A
ENST00000705255.1:n.1692-16384G>A
ENST00000400926.5:c.-98+7640G>A	ENSP00000383715.2:n.-98+7640G>A
NM_004367.5:c.-98+7640G>A	NP_004358.2:n.-98+7640G>A
XR_943250.1:n.2941C>T
XR_943251.1:n.2941C>T
XR_001744467.2:n.1188-312C>T
XR_001744469.2:n.1118-312C>T
XR_943250.3:n.2708C>T
XR_943251.3:n.2949C>T
NM_004367.6:c.-98+7640G>A	NP_004358.2:n.-98+7640G>A