Canonical Allele Identifier: CA2681197692
Gene: CCR6 HGNC NCBI

Linked Data

gnomAD v4: 6-167119224-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167119224C>A , CM000668.2:g.167119224C>A GRCh38
NC_000006.11:g.167532712C>A , CM000668.1:g.167532712C>A GRCh37
NC_000006.10:g.167452702C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609590.2:n.2170-15710C>A
ENST00000705249.1:c.1066-16814C>A ENSP00000516101.1:n.1066-16814C>A
ENST00000705250.1:c.844-16814C>A ENSP00000516102.1:n.844-16814C>A
ENST00000705251.1:c.*713-16814C>A ENSP00000516103.1:n.*713-16814C>A
ENST00000705252.1:c.*536-16814C>A ENSP00000516104.1:n.*536-16814C>A
ENST00000705253.1:c.*536-16814C>A ENSP00000516105.1:n.*536-16814C>A
ENST00000705254.1:c.673-16814C>A ENSP00000516106.1:n.673-16814C>A
ENST00000705255.1:n.1692-16814C>A
ENST00000400926.5:c.-98+7210C>A ENSP00000383715.2:n.-98+7210C>A
NM_004367.5:c.-98+7210C>A NP_004358.2:n.-98+7210C>A
XR_943250.1:n.3371G>T
XR_943251.1:n.3371G>T
XR_001744467.2:n.1306G>T
XR_001744469.2:n.1236G>T
XR_943250.3:n.3138G>T
XR_943251.3:n.3379G>T
NM_004367.6:c.-98+7210C>A NP_004358.2:n.-98+7210C>A
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