Canonical Allele Identifier: CA1363722

Gene: IL10

Linked Data

• ClinVar Variation Id: 1917191
• ClinVar RCV Id: RCV002598079
• dbSNP Id: rs142726516
• ExAC: 1:206941989 G / A
• gnomAD v2: 1-206941989-G-A
• gnomAD v3: 1-206768644-G-A
• gnomAD v4: 1-206768644-G-A
• MyVariant Identifiers: chr1:g.206941989G>A (hg19) ; chr1:g.206768644G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768644G>A , CM000663.2:g.206768644G>A	GRCh38
NC_000001.10:g.206941989G>A , CM000663.1:g.206941989G>A	GRCh37
NC_000001.9:g.205008612G>A	NCBI36
NG_012088.1:g.8851C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1534C>T
ENST00000471071.2:c.274C>T	ENSP00000493073.2:p.Arg92Ter
ENST00000640756.2:n.339C>T
ENST00000659065.2:c.412C>T	ENSP00000499588.1:p.Arg138Ter
ENST00000659642.2:c.412C>T	ENSP00000499509.1:p.Arg138Ter
ENST00000664374.2:c.412C>T	ENSP00000499664.1:p.Arg138Ter
ENST00000640756.1:n.328C>T
ENST00000659065.1:c.412C>T	ENSP00000499588.1:p.Arg138Ter
ENST00000659642.1:c.412C>T	ENSP00000499509.1:p.Arg138Ter
ENST00000664374.1:c.412C>T	ENSP00000499664.1:p.Arg138Ter
ENST00000423557.1:c.529C>T MANE Select	ENSP00000412237.1:p.Arg177Ter
NM_000572.2:c.529C>T	NP_000563.1:p.Arg177Ter
XM_011509506.1:c.529C>T	XP_011507808.1:p.Arg177Ter
NM_000572.3:c.529C>T MANE Select	NP_000563.1:p.Arg177Ter
NM_001382624.1:c.274C>T	NP_001369553.1:p.Arg92Ter
NR_168466.1:n.826C>T
NR_168467.1:n.356C>T