Canonical Allele Identifier: CA822270548

Gene: CCR6

Linked Data

• dbSNP Id: rs1189487408
• MyVariant Identifiers: chr6:g.167533029A>C (hg19) ; chr6:g.167119541A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119541A>C , CM000668.2:g.167119541A>C	GRCh38
NC_000006.11:g.167533029A>C , CM000668.1:g.167533029A>C	GRCh37
NC_000006.10:g.167453019A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-15393A>C
ENST00000705249.1:c.1066-16497A>C	ENSP00000516101.1:n.1066-16497A>C
ENST00000705250.1:c.844-16497A>C	ENSP00000516102.1:n.844-16497A>C
ENST00000705251.1:c.*713-16497A>C	ENSP00000516103.1:n.*713-16497A>C
ENST00000705252.1:c.*536-16497A>C	ENSP00000516104.1:n.*536-16497A>C
ENST00000705253.1:c.*536-16497A>C	ENSP00000516105.1:n.*536-16497A>C
ENST00000705254.1:c.673-16497A>C	ENSP00000516106.1:n.673-16497A>C
ENST00000705255.1:n.1692-16497A>C
ENST00000400926.5:c.-98+7527A>C	ENSP00000383715.2:n.-98+7527A>C
NM_004367.5:c.-98+7527A>C	NP_004358.2:n.-98+7527A>C
XR_943250.1:n.3054T>G
XR_943251.1:n.3054T>G
XR_001744467.2:n.1188-199T>G
XR_001744469.2:n.1118-199T>G
XR_943250.3:n.2821T>G
XR_943251.3:n.3062T>G
NM_004367.6:c.-98+7527A>C	NP_004358.2:n.-98+7527A>C