Canonical Allele Identifier: CA11100590
Gene: CCL20 HGNC NCBI
MyVariant.info:
GRCh38 chr2:g.227805859G>A
GRCh37 chr2:g.228670575G>A
gnomAD v2:
2:228670575 G / A
gnomAD v3:
2:227805859 G / A
gnomAD v4:
chr2-227805859-G-A
Joint Max Group AF 0.78866158 (EAS)
Genomes Max Group AF 0.78866158 (EAS)
Exomes Max Group AF 0.2044221 (NFE)
dbSNP:
10175070
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.227805859G>A , CM000664.2:g.227805859G>A GRCh38
NC_000002.11:g.228670575G>A , CM000664.1:g.228670575G>A GRCh37
NC_000002.10:g.228378819G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000646475.1:c.-201G>A ENSP00000496658.1:n.-201G>A
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