Canonical Allele Identifier: CA151946928

Gene: CCR6

Linked Data

• dbSNP Id: rs978840901
• gnomAD v2: 6-167525987-G-C
• gnomAD v3: 6-167112499-G-C
• gnomAD v4: 6-167112499-G-C
• MyVariant Identifiers: chr6:g.167525987G>C (hg19) ; chr6:g.167112499G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167112499G>C , CM000668.2:g.167112499G>C	GRCh38
NC_000006.11:g.167525987G>C , CM000668.1:g.167525987G>C	GRCh37
NC_000006.10:g.167445977G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-22435G>C
ENST00000705249.1:c.1066-23539G>C	ENSP00000516101.1:n.1066-23539G>C
ENST00000705250.1:c.844-23539G>C	ENSP00000516102.1:n.844-23539G>C
ENST00000705251.1:c.*713-23539G>C	ENSP00000516103.1:n.*713-23539G>C
ENST00000705252.1:c.*536-23539G>C	ENSP00000516104.1:n.*536-23539G>C
ENST00000705253.1:c.*536-23539G>C	ENSP00000516105.1:n.*536-23539G>C
ENST00000705254.1:c.673-23539G>C	ENSP00000516106.1:n.673-23539G>C
ENST00000705255.1:n.1692-23539G>C
ENST00000400926.5:c.-98+485G>C	ENSP00000383715.2:n.-98+485G>C
NM_004367.5:c.-98+485G>C	NP_004358.2:n.-98+485G>C
XR_943250.1:n.7998C>G
XR_943251.1:n.7417C>G
XR_001744467.2:n.5933C>G
XR_001744469.2:n.5863C>G
XR_943250.3:n.7765C>G
XR_943251.3:n.7425C>G
NM_004367.6:c.-98+485G>C	NP_004358.2:n.-98+485G>C