Canonical Allele Identifier: CA151949729

Gene: CCR6

Linked Data

• dbSNP Id: rs77958989
• MyVariant Identifiers: chr6:g.167533040G>C (hg19) ; chr6:g.167119552G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119552G>C , CM000668.2:g.167119552G>C	GRCh38
NC_000006.11:g.167533040G>C , CM000668.1:g.167533040G>C	GRCh37
NC_000006.10:g.167453030G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-15382G>C
ENST00000705249.1:c.1066-16486G>C	ENSP00000516101.1:n.1066-16486G>C
ENST00000705250.1:c.844-16486G>C	ENSP00000516102.1:n.844-16486G>C
ENST00000705251.1:c.*713-16486G>C	ENSP00000516103.1:n.*713-16486G>C
ENST00000705252.1:c.*536-16486G>C	ENSP00000516104.1:n.*536-16486G>C
ENST00000705253.1:c.*536-16486G>C	ENSP00000516105.1:n.*536-16486G>C
ENST00000705254.1:c.673-16486G>C	ENSP00000516106.1:n.673-16486G>C
ENST00000705255.1:n.1692-16486G>C
ENST00000400926.5:c.-98+7538G>C	ENSP00000383715.2:n.-98+7538G>C
NM_004367.5:c.-98+7538G>C	NP_004358.2:n.-98+7538G>C
XR_943250.1:n.3043C>G
XR_943251.1:n.3043C>G
XR_001744467.2:n.1188-210C>G
XR_001744469.2:n.1118-210C>G
XR_943250.3:n.2810C>G
XR_943251.3:n.3051C>G
NM_004367.6:c.-98+7538G>C	NP_004358.2:n.-98+7538G>C