Canonical Allele Identifier: CA151946954

Gene: CCR6

Linked Data

• dbSNP Id: rs1036130313
• MyVariant Identifiers: chr6:g.167526063C>T (hg19) ; chr6:g.167112575C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167112575C>T , CM000668.2:g.167112575C>T	GRCh38
NC_000006.11:g.167526063C>T , CM000668.1:g.167526063C>T	GRCh37
NC_000006.10:g.167446053C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-22359C>T
ENST00000705249.1:c.1066-23463C>T	ENSP00000516101.1:n.1066-23463C>T
ENST00000705250.1:c.844-23463C>T	ENSP00000516102.1:n.844-23463C>T
ENST00000705251.1:c.*713-23463C>T	ENSP00000516103.1:n.*713-23463C>T
ENST00000705252.1:c.*536-23463C>T	ENSP00000516104.1:n.*536-23463C>T
ENST00000705253.1:c.*536-23463C>T	ENSP00000516105.1:n.*536-23463C>T
ENST00000705254.1:c.673-23463C>T	ENSP00000516106.1:n.673-23463C>T
ENST00000705255.1:n.1692-23463C>T
ENST00000400926.5:c.-98+561C>T	ENSP00000383715.2:n.-98+561C>T
NM_004367.5:c.-98+561C>T	NP_004358.2:n.-98+561C>T
XR_943250.1:n.7922G>A
XR_943251.1:n.7341G>A
XR_001744467.2:n.5857G>A
XR_001744469.2:n.5787G>A
XR_943250.3:n.7689G>A
XR_943251.3:n.7349G>A
NM_004367.6:c.-98+561C>T	NP_004358.2:n.-98+561C>T