Canonical Allele Identifier: CA2606067667

Gene: CCR6

Linked Data

• dbSNP Id: rs2114906341
• gnomAD v3: 6-167112583-C-A
• gnomAD v4: 6-167112583-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167112583C>A , CM000668.2:g.167112583C>A	GRCh38
NC_000006.11:g.167526071C>A , CM000668.1:g.167526071C>A	GRCh37
NC_000006.10:g.167446061C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-22351C>A
ENST00000705249.1:c.1066-23455C>A	ENSP00000516101.1:n.1066-23455C>A
ENST00000705250.1:c.844-23455C>A	ENSP00000516102.1:n.844-23455C>A
ENST00000705251.1:c.*713-23455C>A	ENSP00000516103.1:n.*713-23455C>A
ENST00000705252.1:c.*536-23455C>A	ENSP00000516104.1:n.*536-23455C>A
ENST00000705253.1:c.*536-23455C>A	ENSP00000516105.1:n.*536-23455C>A
ENST00000705254.1:c.673-23455C>A	ENSP00000516106.1:n.673-23455C>A
ENST00000705255.1:n.1692-23455C>A
ENST00000400926.5:c.-98+569C>A	ENSP00000383715.2:n.-98+569C>A
NM_004367.5:c.-98+569C>A	NP_004358.2:n.-98+569C>A
XR_943250.1:n.7914G>T
XR_943251.1:n.7333G>T
XR_001744467.2:n.5849G>T
XR_001744469.2:n.5779G>T
XR_943250.3:n.7681G>T
XR_943251.3:n.7341G>T
NM_004367.6:c.-98+569C>A	NP_004358.2:n.-98+569C>A