Canonical Allele Identifier: CA822270587

Gene: CCR6

Linked Data

• dbSNP Id: rs1192427139
• gnomAD v3: 6-167119624-G-A
• gnomAD v4: 6-167119624-G-A
• MyVariant Identifiers: chr6:g.167533112G>A (hg19) ; chr6:g.167119624G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119624G>A , CM000668.2:g.167119624G>A	GRCh38
NC_000006.11:g.167533112G>A , CM000668.1:g.167533112G>A	GRCh37
NC_000006.10:g.167453102G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-15310G>A
ENST00000705249.1:c.1066-16414G>A	ENSP00000516101.1:n.1066-16414G>A
ENST00000705250.1:c.844-16414G>A	ENSP00000516102.1:n.844-16414G>A
ENST00000705251.1:c.*713-16414G>A	ENSP00000516103.1:n.*713-16414G>A
ENST00000705252.1:c.*536-16414G>A	ENSP00000516104.1:n.*536-16414G>A
ENST00000705253.1:c.*536-16414G>A	ENSP00000516105.1:n.*536-16414G>A
ENST00000705254.1:c.673-16414G>A	ENSP00000516106.1:n.673-16414G>A
ENST00000705255.1:n.1692-16414G>A
ENST00000400926.5:c.-98+7610G>A	ENSP00000383715.2:n.-98+7610G>A
NM_004367.5:c.-98+7610G>A	NP_004358.2:n.-98+7610G>A
XR_943250.1:n.2971C>T
XR_943251.1:n.2971C>T
XR_001744467.2:n.1188-282C>T
XR_001744469.2:n.1118-282C>T
XR_943250.3:n.2738C>T
XR_943251.3:n.2979C>T
NM_004367.6:c.-98+7610G>A	NP_004358.2:n.-98+7610G>A