Canonical Allele Identifier: CA151946968

Gene: CCR6

Linked Data

• dbSNP Id: rs145501643
• gnomAD v3: 6-167112596-G-A
• gnomAD v4: 6-167112596-G-A
• MyVariant Identifiers: chr6:g.167526084G>A (hg19) ; chr6:g.167112596G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167112596G>A , CM000668.2:g.167112596G>A	GRCh38
NC_000006.11:g.167526084G>A , CM000668.1:g.167526084G>A	GRCh37
NC_000006.10:g.167446074G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-22338G>A
ENST00000705249.1:c.1066-23442G>A	ENSP00000516101.1:n.1066-23442G>A
ENST00000705250.1:c.844-23442G>A	ENSP00000516102.1:n.844-23442G>A
ENST00000705251.1:c.*713-23442G>A	ENSP00000516103.1:n.*713-23442G>A
ENST00000705252.1:c.*536-23442G>A	ENSP00000516104.1:n.*536-23442G>A
ENST00000705253.1:c.*536-23442G>A	ENSP00000516105.1:n.*536-23442G>A
ENST00000705254.1:c.673-23442G>A	ENSP00000516106.1:n.673-23442G>A
ENST00000705255.1:n.1692-23442G>A
ENST00000400926.5:c.-98+582G>A	ENSP00000383715.2:n.-98+582G>A
NM_004367.5:c.-98+582G>A	NP_004358.2:n.-98+582G>A
XR_943250.1:n.7901C>T
XR_943251.1:n.7320C>T
XR_001744467.2:n.5836C>T
XR_001744469.2:n.5766C>T
XR_943250.3:n.7668C>T
XR_943251.3:n.7328C>T
NM_004367.6:c.-98+582G>A	NP_004358.2:n.-98+582G>A