Canonical Allele Identifier: CA1097031969

Gene: CCR6

Linked Data

• dbSNP Id: rs1722168499
• gnomAD v3: 6-167119487-T-G
• gnomAD v4: 6-167119487-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119487T>G , CM000668.2:g.167119487T>G	GRCh38
NC_000006.11:g.167532975T>G , CM000668.1:g.167532975T>G	GRCh37
NC_000006.10:g.167452965T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-15447T>G
ENST00000705249.1:c.1066-16551T>G	ENSP00000516101.1:n.1066-16551T>G
ENST00000705250.1:c.844-16551T>G	ENSP00000516102.1:n.844-16551T>G
ENST00000705251.1:c.*713-16551T>G	ENSP00000516103.1:n.*713-16551T>G
ENST00000705252.1:c.*536-16551T>G	ENSP00000516104.1:n.*536-16551T>G
ENST00000705253.1:c.*536-16551T>G	ENSP00000516105.1:n.*536-16551T>G
ENST00000705254.1:c.673-16551T>G	ENSP00000516106.1:n.673-16551T>G
ENST00000705255.1:n.1692-16551T>G
ENST00000400926.5:c.-98+7473T>G	ENSP00000383715.2:n.-98+7473T>G
NM_004367.5:c.-98+7473T>G	NP_004358.2:n.-98+7473T>G
XR_943250.1:n.3108A>C
XR_943251.1:n.3108A>C
XR_001744467.2:n.1188-145A>C
XR_001744469.2:n.1118-145A>C
XR_943250.3:n.2875A>C
XR_943251.3:n.3116A>C
NM_004367.6:c.-98+7473T>G	NP_004358.2:n.-98+7473T>G