Canonical Allele Identifier: CA151947011

Gene: CCR6

Linked Data

• dbSNP Id: rs557814172
• MyVariant Identifiers: chr6:g.167526157G>A (hg19) ; chr6:g.167112669G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167112669G>A , CM000668.2:g.167112669G>A	GRCh38
NC_000006.11:g.167526157G>A , CM000668.1:g.167526157G>A	GRCh37
NC_000006.10:g.167446147G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-22265G>A
ENST00000705249.1:c.1066-23369G>A	ENSP00000516101.1:n.1066-23369G>A
ENST00000705250.1:c.844-23369G>A	ENSP00000516102.1:n.844-23369G>A
ENST00000705251.1:c.*713-23369G>A	ENSP00000516103.1:n.*713-23369G>A
ENST00000705252.1:c.*536-23369G>A	ENSP00000516104.1:n.*536-23369G>A
ENST00000705253.1:c.*536-23369G>A	ENSP00000516105.1:n.*536-23369G>A
ENST00000705254.1:c.673-23369G>A	ENSP00000516106.1:n.673-23369G>A
ENST00000705255.1:n.1692-23369G>A
ENST00000400926.5:c.-98+655G>A	ENSP00000383715.2:n.-98+655G>A
NM_004367.5:c.-98+655G>A	NP_004358.2:n.-98+655G>A
XR_943250.1:n.7828C>T
XR_943251.1:n.7247C>T
XR_001744467.2:n.5763C>T
XR_001744469.2:n.5693C>T
XR_943250.3:n.7595C>T
XR_943251.3:n.7255C>T
NM_004367.6:c.-98+655G>A	NP_004358.2:n.-98+655G>A