Canonical Allele Identifier: CA2681197679

Gene: CCR6

Linked Data

• gnomAD v4: 6-167119217-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.167119217G>T , CM000668.2:g.167119217G>T	GRCh38
NC_000006.11:g.167532705G>T , CM000668.1:g.167532705G>T	GRCh37
NC_000006.10:g.167452695G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609590.2:n.2170-15717G>T
ENST00000705249.1:c.1066-16821G>T	ENSP00000516101.1:n.1066-16821G>T
ENST00000705250.1:c.844-16821G>T	ENSP00000516102.1:n.844-16821G>T
ENST00000705251.1:c.*713-16821G>T	ENSP00000516103.1:n.*713-16821G>T
ENST00000705252.1:c.*536-16821G>T	ENSP00000516104.1:n.*536-16821G>T
ENST00000705253.1:c.*536-16821G>T	ENSP00000516105.1:n.*536-16821G>T
ENST00000705254.1:c.673-16821G>T	ENSP00000516106.1:n.673-16821G>T
ENST00000705255.1:n.1692-16821G>T
ENST00000400926.5:c.-98+7203G>T	ENSP00000383715.2:n.-98+7203G>T
NM_004367.5:c.-98+7203G>T	NP_004358.2:n.-98+7203G>T
XR_943250.1:n.3378C>A
XR_943251.1:n.3378C>A
XR_001744467.2:n.1313C>A
XR_001744469.2:n.1243C>A
XR_943250.3:n.3145C>A
XR_943251.3:n.3386C>A
NM_004367.6:c.-98+7203G>T	NP_004358.2:n.-98+7203G>T