Canonical Allele Identifier: CA12381538
Gene: CCR6 HGNC NCBI

Linked Data

dbSNP Id: rs1854853

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167119574A>G , CM000668.2:g.167119574A>G GRCh38
NC_000006.11:g.167533062A>G , CM000668.1:g.167533062A>G GRCh37
NC_000006.10:g.167453052A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000400926.5:c.-98+7560A>G ENSP00000383715.2:p.=
NM_004367.5:c.-98+7560A>G NP_004358.2:p.=
XR_943250.1:n.3021T>C
XR_943251.1:n.3021T>C
XR_001744467.2:n.1188-232T>C
XR_001744469.2:n.1118-232T>C
XR_943250.3:n.2788T>C
XR_943251.3:n.3029T>C
NM_004367.6:c.-98+7560A>G NP_004358.2:p.=