Canonical Allele Identifier: CA151949759

Gene: CCR6

Linked Data

• dbSNP Id: rs530239408
• gnomAD v2: 6-167533080-C-T
• gnomAD v3: 6-167119592-C-T
• gnomAD v4: 6-167119592-C-T
• MyVariant Identifiers: chr6:g.167533080C>T (hg19) ; chr6:g.167119592C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119592C>T , CM000668.2:g.167119592C>T	GRCh38
NC_000006.11:g.167533080C>T , CM000668.1:g.167533080C>T	GRCh37
NC_000006.10:g.167453070C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-15342C>T
ENST00000705249.1:c.1066-16446C>T	ENSP00000516101.1:n.1066-16446C>T
ENST00000705250.1:c.844-16446C>T	ENSP00000516102.1:n.844-16446C>T
ENST00000705251.1:c.*713-16446C>T	ENSP00000516103.1:n.*713-16446C>T
ENST00000705252.1:c.*536-16446C>T	ENSP00000516104.1:n.*536-16446C>T
ENST00000705253.1:c.*536-16446C>T	ENSP00000516105.1:n.*536-16446C>T
ENST00000705254.1:c.673-16446C>T	ENSP00000516106.1:n.673-16446C>T
ENST00000705255.1:n.1692-16446C>T
ENST00000400926.5:c.-98+7578C>T	ENSP00000383715.2:n.-98+7578C>T
NM_004367.5:c.-98+7578C>T	NP_004358.2:n.-98+7578C>T
XR_943250.1:n.3003G>A
XR_943251.1:n.3003G>A
XR_001744467.2:n.1188-250G>A
XR_001744469.2:n.1118-250G>A
XR_943250.3:n.2770G>A
XR_943251.3:n.3011G>A
NM_004367.6:c.-98+7578C>T	NP_004358.2:n.-98+7578C>T