Canonical Allele Identifier: CA822266801

Gene: CCR6

Linked Data

• dbSNP Id: rs1197417234
• gnomAD v3: 6-167112446-G-C
• gnomAD v4: 6-167112446-G-C
• MyVariant Identifiers: chr6:g.167525934G>C (hg19) ; chr6:g.167112446G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167112446G>C , CM000668.2:g.167112446G>C	GRCh38
NC_000006.11:g.167525934G>C , CM000668.1:g.167525934G>C	GRCh37
NC_000006.10:g.167445924G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-22488G>C
ENST00000705249.1:c.1066-23592G>C	ENSP00000516101.1:n.1066-23592G>C
ENST00000705250.1:c.844-23592G>C	ENSP00000516102.1:n.844-23592G>C
ENST00000705251.1:c.*713-23592G>C	ENSP00000516103.1:n.*713-23592G>C
ENST00000705252.1:c.*536-23592G>C	ENSP00000516104.1:n.*536-23592G>C
ENST00000705253.1:c.*536-23592G>C	ENSP00000516105.1:n.*536-23592G>C
ENST00000705254.1:c.673-23592G>C	ENSP00000516106.1:n.673-23592G>C
ENST00000705255.1:n.1692-23592G>C
ENST00000400926.5:c.-98+432G>C	ENSP00000383715.2:n.-98+432G>C
NM_004367.5:c.-98+432G>C	NP_004358.2:n.-98+432G>C
XR_943250.1:n.8051C>G
XR_943251.1:n.7470C>G
XR_001744467.2:n.5986C>G
XR_001744469.2:n.5916C>G
XR_943250.3:n.7818C>G
XR_943251.3:n.7478C>G
NM_004367.6:c.-98+432G>C	NP_004358.2:n.-98+432G>C