Canonical Allele Identifier: CA151948855

Gene: CCR6

Linked Data

• dbSNP Id: rs945929740
• gnomAD v3: 6-167135075-C-T
• gnomAD v4: 6-167135075-C-T
• MyVariant Identifiers: chr6:g.167548563C>T (hg19) ; chr6:g.167135075C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167135075C>T , CM000668.2:g.167135075C>T	GRCh38
NC_000006.11:g.167548563C>T , CM000668.1:g.167548563C>T	GRCh37
NC_000006.10:g.167468553C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2302+9C>T
ENST00000705249.1:c.1066-963C>T	ENSP00000516101.1:n.1066-963C>T
ENST00000705250.1:c.844-963C>T	ENSP00000516102.1:n.844-963C>T
ENST00000705251.1:c.*713-963C>T	ENSP00000516103.1:n.*713-963C>T
ENST00000705252.1:c.*536-963C>T	ENSP00000516104.1:n.*536-963C>T
ENST00000705253.1:c.*536-963C>T	ENSP00000516105.1:n.*536-963C>T
ENST00000705254.1:c.673-963C>T	ENSP00000516106.1:n.673-963C>T
ENST00000705255.1:n.1692-963C>T
ENST00000341935.10:c.-97-963C>T MANE Select	ENSP00000343952.5:n.-97-963C>T
ENST00000643861.1:c.-97-963C>T	ENSP00000493637.1:n.-97-963C>T
ENST00000341935.9:c.-97-963C>T	ENSP00000343952.5:n.-97-963C>T
ENST00000349984.6:c.-97-963C>T	ENSP00000339393.4:n.-97-963C>T
ENST00000400926.5:c.-97-963C>T	ENSP00000383715.2:n.-97-963C>T
NM_004367.5:c.-97-963C>T	NP_004358.2:n.-97-963C>T
NM_031409.3:c.-97-963C>T	NP_113597.2:n.-97-963C>T
NM_004367.6:c.-97-963C>T	NP_004358.2:n.-97-963C>T
NM_031409.4:c.-97-963C>T MANE Select	NP_113597.2:n.-97-963C>T
NM_001394582.1:c.-97-963C>T	NP_001381511.1:n.-97-963C>T