Canonical Allele Identifier: CA12434900
Gene: CCR6 HGNC NCBI

Linked Data

dbSNP Id: rs62436827

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.167135059A>G , CM000668.2:g.167135059A>G GRCh38
NC_000006.11:g.167548547A>G , CM000668.1:g.167548547A>G GRCh37
NC_000006.10:g.167468537A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000643861.1:c.-97-979A>G ENSP00000493637.1:p.=
ENST00000341935.9:c.-97-979A>G ENSP00000343952.5:p.=
ENST00000349984.6:c.-97-979A>G ENSP00000339393.4:p.=
ENST00000400926.5:c.-97-979A>G ENSP00000383715.2:p.=
NM_004367.5:c.-97-979A>G NP_004358.2:p.=
NM_031409.3:c.-97-979A>G NP_113597.2:p.=
NM_004367.6:c.-97-979A>G NP_004358.2:p.=
NM_031409.4:c.-97-979A>G NP_113597.2:p.=