Canonical Allele Identifier: CA822266778

Gene: CCR6

Linked Data

• dbSNP Id: rs1465185307
• MyVariant Identifiers: chr6:g.167525906A>C (hg19) ; chr6:g.167112418A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167112418A>C , CM000668.2:g.167112418A>C	GRCh38
NC_000006.11:g.167525906A>C , CM000668.1:g.167525906A>C	GRCh37
NC_000006.10:g.167445896A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609590.2:n.2170-22516A>C
ENST00000705249.1:c.1066-23620A>C	ENSP00000516101.1:n.1066-23620A>C
ENST00000705250.1:c.844-23620A>C	ENSP00000516102.1:n.844-23620A>C
ENST00000705251.1:c.*713-23620A>C	ENSP00000516103.1:n.*713-23620A>C
ENST00000705252.1:c.*536-23620A>C	ENSP00000516104.1:n.*536-23620A>C
ENST00000705253.1:c.*536-23620A>C	ENSP00000516105.1:n.*536-23620A>C
ENST00000705254.1:c.673-23620A>C	ENSP00000516106.1:n.673-23620A>C
ENST00000705255.1:n.1692-23620A>C
ENST00000400926.5:c.-98+404A>C	ENSP00000383715.2:n.-98+404A>C
NM_004367.5:c.-98+404A>C	NP_004358.2:n.-98+404A>C
XR_943250.1:n.8079T>G
XR_943251.1:n.7498T>G
XR_001744467.2:n.6014T>G
XR_001744469.2:n.5944T>G
XR_943250.3:n.7846T>G
XR_943251.3:n.7506T>G
NM_004367.6:c.-98+404A>C	NP_004358.2:n.-98+404A>C