Canonical Allele Identifier: CA1680249725

Gene: CCR6

Linked Data

• dbSNP Id: rs1781546876

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119122del , CM000668.2:g.167119122del	GRCh38
NC_000006.11:g.167532610del , CM000668.1:g.167532610del	GRCh37
NC_000006.10:g.167452600del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-15812del
ENST00000705249.1:c.1066-16916del	ENSP00000516101.1:n.1066-16916del
ENST00000705250.1:c.844-16916del	ENSP00000516102.1:n.844-16916del
ENST00000705251.1:c.*713-16916del	ENSP00000516103.1:n.*713-16916del
ENST00000705252.1:c.*536-16916del	ENSP00000516104.1:n.*536-16916del
ENST00000705253.1:c.*536-16916del	ENSP00000516105.1:n.*536-16916del
ENST00000705254.1:c.673-16916del	ENSP00000516106.1:n.673-16916del
ENST00000705255.1:n.1692-16916del
ENST00000400926.5:c.-98+7108del	ENSP00000383715.2:n.-98+7108del
NM_004367.5:c.-98+7108del	NP_004358.2:n.-98+7108del
XR_943250.1:n.3409+65del
XR_943251.1:n.3409+65del
XR_001744467.2:n.1344+65del
XR_001744469.2:n.1274+65del
XR_943250.3:n.3176+65del
XR_943251.3:n.3417+65del
NM_004367.6:c.-98+7108del	NP_004358.2:n.-98+7108del