Canonical Allele Identifier: CA10889963
Gene: IL20 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.206865341C>T
GRCh37 chr1:g.207038686C>T
gnomAD v2:
1:207038686 C / T
gnomAD v3:
1:206865341 C / T
gnomAD v4:
chr1-206865341-C-T
Joint Max Group AF 0.36605069 (AFR)
Genomes Max Group AF 0.36515229 (AFR)
Exomes Max Group AF 0.37203544 (AFR)
dbSNP:
1400986
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206865341C>T , CM000663.2:g.206865341C>T GRCh38
NC_000001.10:g.207038686C>T , CM000663.1:g.207038686C>T GRCh37
NC_000001.9:g.205105309C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_005273152.3:c.-121C>T XP_005273209.1:n.-121C>T
NM_001385166.1:c.-170-206C>T NP_001372095.1:n.-170-206C>T
NM_001385167.1:c.-251-5C>T NP_001372096.1:n.-251-5C>T
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