Canonical Allele Identifier: CA36575858
Gene: IL20 HGNC NCBI
COSMIC:
COSN6439158 (not active)
MyVariant.info:
GRCh38 chr1:g.206864130G>C
GRCh37 chr1:g.207037475G>C
gnomAD v2:
1:207037475 G / C
gnomAD v3:
1:206864130 G / C
gnomAD v4:
chr1-206864130-G-C
Joint Max Group AF 0.95267911 (AFR)
Genomes Max Group AF 0.95267911 (AFR)
dbSNP:
1713239
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206864130G>C , CM000663.2:g.206864130G>C GRCh38
NC_000001.10:g.207037475G>C , CM000663.1:g.207037475G>C GRCh37
NC_000001.9:g.205104098G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001385166.1:c.-171+523G>C NP_001372095.1:n.-171+523G>C
NM_001385167.1:c.-252+523G>C NP_001372096.1:n.-252+523G>C
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