Canonical Allele Identifier: CA6298833

Gene: IL10RA

Linked Data

• ClinVar Variation Id: 302536
• ClinVar RCV Id: RCV000593830 ; RCV001088383
• dbSNP Id: rs377525753
• ExAC: 11:117859125 G / A
• gnomAD v2: 11-117859125-G-A
• gnomAD v3: 11-117988410-G-A
• gnomAD v4: 11-117988410-G-A
• MyVariant Identifiers: chr11:g.117859125G>A (hg19) ; chr11:g.117988410G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.117988410G>A , CM000673.2:g.117988410G>A	GRCh38
NC_000011.9:g.117859125G>A , CM000673.1:g.117859125G>A	GRCh37
NC_000011.8:g.117364335G>A	NCBI36
NG_016275.1:g.7020G>A , LRG_151:g.7020G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525467.2:n.444G>A
ENST00000696732.1:n.1945G>A
ENST00000227752.8:c.96G>A MANE Select	ENSP00000227752.4:p.Val32=
ENST00000529924.6:n.1674G>A
ENST00000227752.7:c.96G>A	ENSP00000227752.3:p.Val32=
ENST00000526544.5:c.96G>A	ENSP00000435317.1:p.Val32=
ENST00000529924.5:n.1674G>A
ENST00000530761.5:n.473G>A
ENST00000531365.1:n.123G>A
ENST00000533700.5:n.303G>A
ENST00000534574.5:c.*36G>A	ENSP00000436328.1:n.*36G>A
NM_001558.3:c.96G>A , LRG_151t1:c.96G>A	NP_001549.2:p.Val32=
NR_026691.1:n.303G>A
XM_024448493.1:c.-173G>A	XP_024304261.1:n.-173G>A
NM_001558.4:c.96G>A MANE Select	NP_001549.2:p.Val32=
NR_026691.2:n.300G>A