Canonical Allele Identifier: CA10889963

Gene: IL20

Linked Data

• dbSNP Id: rs1400986
• gnomAD v2: 1-207038686-C-T
• gnomAD v3: 1-206865341-C-T
• gnomAD v4: 1-206865341-C-T
• MyVariant Identifiers: chr1:g.207038686C>T (hg19) ; chr1:g.206865341C>T (hg38)

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