Canonical Allele Identifier: CA822266840

Gene: CCR6

Linked Data

• dbSNP Id: rs1158882498
• MyVariant Identifiers: chr6:g.167526045T>C (hg19) ; chr6:g.167112557T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167112557T>C , CM000668.2:g.167112557T>C	GRCh38
NC_000006.11:g.167526045T>C , CM000668.1:g.167526045T>C	GRCh37
NC_000006.10:g.167446035T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-22377T>C
ENST00000705249.1:c.1066-23481T>C	ENSP00000516101.1:n.1066-23481T>C
ENST00000705250.1:c.844-23481T>C	ENSP00000516102.1:n.844-23481T>C
ENST00000705251.1:c.*713-23481T>C	ENSP00000516103.1:n.*713-23481T>C
ENST00000705252.1:c.*536-23481T>C	ENSP00000516104.1:n.*536-23481T>C
ENST00000705253.1:c.*536-23481T>C	ENSP00000516105.1:n.*536-23481T>C
ENST00000705254.1:c.673-23481T>C	ENSP00000516106.1:n.673-23481T>C
ENST00000705255.1:n.1692-23481T>C
ENST00000400926.5:c.-98+543T>C	ENSP00000383715.2:n.-98+543T>C
NM_004367.5:c.-98+543T>C	NP_004358.2:n.-98+543T>C
XR_943250.1:n.7940A>G
XR_943251.1:n.7359A>G
XR_001744467.2:n.5875A>G
XR_001744469.2:n.5805A>G
XR_943250.3:n.7707A>G
XR_943251.3:n.7367A>G
NM_004367.6:c.-98+543T>C	NP_004358.2:n.-98+543T>C