Canonical Allele Identifier: CA151953355

Gene: CCR6

Linked Data

• dbSNP Id: rs181478053
• gnomAD v2: 6-167540649-G-C
• gnomAD v3: 6-167127161-G-C
• gnomAD v4: 6-167127161-G-C
• MyVariant Identifiers: chr6:g.167540649G>C (hg19) ; chr6:g.167127161G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167127161G>C , CM000668.2:g.167127161G>C	GRCh38
NC_000006.11:g.167540649G>C , CM000668.1:g.167540649G>C	GRCh37
NC_000006.10:g.167460639G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-7773G>C
ENST00000705249.1:c.1066-8877G>C	ENSP00000516101.1:n.1066-8877G>C
ENST00000705250.1:c.844-8877G>C	ENSP00000516102.1:n.844-8877G>C
ENST00000705251.1:c.*713-8877G>C	ENSP00000516103.1:n.*713-8877G>C
ENST00000705252.1:c.*536-8877G>C	ENSP00000516104.1:n.*536-8877G>C
ENST00000705253.1:c.*536-8877G>C	ENSP00000516105.1:n.*536-8877G>C
ENST00000705254.1:c.673-8877G>C	ENSP00000516106.1:n.673-8877G>C
ENST00000705255.1:n.1692-8877G>C
ENST00000341935.10:c.-98+3938G>C MANE Select	ENSP00000343952.5:n.-98+3938G>C
ENST00000643861.1:c.-98+3938G>C	ENSP00000493637.1:n.-98+3938G>C
ENST00000341935.9:c.-98+3938G>C	ENSP00000343952.5:n.-98+3938G>C
ENST00000349984.6:c.-98+3938G>C	ENSP00000339393.4:n.-98+3938G>C
ENST00000400926.5:c.-97-8877G>C	ENSP00000383715.2:n.-97-8877G>C
NM_004367.5:c.-97-8877G>C	NP_004358.2:n.-97-8877G>C
NM_031409.3:c.-98+3938G>C	NP_113597.2:n.-98+3938G>C
XR_001744470.1:n.1460C>G
NM_004367.6:c.-97-8877G>C	NP_004358.2:n.-97-8877G>C
NM_031409.4:c.-98+3938G>C MANE Select	NP_113597.2:n.-98+3938G>C
NM_001394582.1:c.-98+3938G>C	NP_001381511.1:n.-98+3938G>C