Canonical Allele Identifier: CA151946924

Gene: CCR6

Linked Data

• dbSNP Id: rs1020573365
• gnomAD v2: 6-167525956-G-A
• gnomAD v3: 6-167112468-G-A
• gnomAD v4: 6-167112468-G-A
• MyVariant Identifiers: chr6:g.167525956G>A (hg19) ; chr6:g.167112468G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167112468G>A , CM000668.2:g.167112468G>A	GRCh38
NC_000006.11:g.167525956G>A , CM000668.1:g.167525956G>A	GRCh37
NC_000006.10:g.167445946G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-22466G>A
ENST00000705249.1:c.1066-23570G>A	ENSP00000516101.1:n.1066-23570G>A
ENST00000705250.1:c.844-23570G>A	ENSP00000516102.1:n.844-23570G>A
ENST00000705251.1:c.*713-23570G>A	ENSP00000516103.1:n.*713-23570G>A
ENST00000705252.1:c.*536-23570G>A	ENSP00000516104.1:n.*536-23570G>A
ENST00000705253.1:c.*536-23570G>A	ENSP00000516105.1:n.*536-23570G>A
ENST00000705254.1:c.673-23570G>A	ENSP00000516106.1:n.673-23570G>A
ENST00000705255.1:n.1692-23570G>A
ENST00000400926.5:c.-98+454G>A	ENSP00000383715.2:n.-98+454G>A
NM_004367.5:c.-98+454G>A	NP_004358.2:n.-98+454G>A
XR_943250.1:n.8029C>T
XR_943251.1:n.7448C>T
XR_001744467.2:n.5964C>T
XR_001744469.2:n.5894C>T
XR_943250.3:n.7796C>T
XR_943251.3:n.7456C>T
NM_004367.6:c.-98+454G>A	NP_004358.2:n.-98+454G>A