Canonical Allele Identifier: CA148648821

Gene: IL20RA

Linked Data

• dbSNP Id: rs1003157426
• gnomAD v2: 6-137353699-T-G
• gnomAD v3: 6-137032562-T-G
• gnomAD v4: 6-137032562-T-G
• MyVariant Identifiers: chr6:g.137353699T>G (hg19) ; chr6:g.137032562T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.137032562T>G , CM000668.2:g.137032562T>G	GRCh38
NC_000006.11:g.137353699T>G , CM000668.1:g.137353699T>G	GRCh37
NC_000006.10:g.137395392T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316649.10:c.88+12079A>C MANE Select	ENSP00000314976.5:n.88+12079A>C
ENST00000316649.9:c.88+12079A>C	ENSP00000314976.5:n.88+12079A>C
ENST00000367746.3:c.88+12079A>C	ENSP00000356720.3:n.88+12079A>C
ENST00000367748.4:c.-67+12079A>C	ENSP00000356722.1:n.-67+12079A>C
ENST00000468393.5:c.-67+12079A>C	ENSP00000489177.1:n.-67+12079A>C
ENST00000541547.5:c.-60+11530A>C	ENSP00000437843.1:n.-60+11530A>C
ENST00000635289.1:c.-67+11530A>C	ENSP00000489419.1:n.-67+11530A>C
NM_001278722.1:c.-60+11530A>C	NP_001265651.1:n.-60+11530A>C
NM_001278723.1:c.-67+12079A>C	NP_001265652.1:n.-67+12079A>C
NM_001278724.1:c.-67+12079A>C	NP_001265653.1:n.-67+12079A>C
NM_014432.3:c.88+12079A>C	NP_055247.3:n.88+12079A>C
XM_006715505.2:c.88+12079A>C	XP_006715568.1:n.88+12079A>C
XM_006715506.2:c.-67+11530A>C	XP_006715569.1:n.-67+11530A>C
XM_011535904.1:c.-67+11530A>C	XP_011534206.1:n.-67+11530A>C
XM_011535904.2:c.-67+11530A>C	XP_011534206.1:n.-67+11530A>C
XM_017010954.2:c.88+12079A>C	XP_016866443.1:n.88+12079A>C
XM_017010955.1:c.-60+11530A>C	XP_016866444.1:n.-60+11530A>C
NM_001278724.2:c.-67+12079A>C	NP_001265653.2:n.-67+12079A>C
NM_001278722.2:c.-60+11530A>C	NP_001265651.2:n.-60+11530A>C
NM_001278723.3:c.-67+12079A>C	NP_001265652.2:n.-67+12079A>C
NM_001278724.4:c.-67+12079A>C	NP_001265653.2:n.-67+12079A>C
NM_014432.4:c.88+12079A>C MANE Select	NP_055247.4:n.88+12079A>C