Canonical Allele Identifier: CA36547797

Gene: IL10

Linked Data

• dbSNP Id: rs142726516
• gnomAD v4: 1-206768644-G-C
• MyVariant Identifiers: chr1:g.206941989G>C (hg19) ; chr1:g.206768644G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1534C>G
ENST00000471071.2:c.274C>G	ENSP00000493073.2:p.Arg92Gly
ENST00000640756.2:n.339C>G
ENST00000659065.2:c.412C>G	ENSP00000499588.1:p.Arg138Gly
ENST00000659642.2:c.412C>G	ENSP00000499509.1:p.Arg138Gly
ENST00000664374.2:c.412C>G	ENSP00000499664.1:p.Arg138Gly
ENST00000640756.1:n.328C>G
ENST00000659065.1:c.412C>G	ENSP00000499588.1:p.Arg138Gly
ENST00000659642.1:c.412C>G	ENSP00000499509.1:p.Arg138Gly
ENST00000664374.1:c.412C>G	ENSP00000499664.1:p.Arg138Gly
ENST00000423557.1:c.529C>G MANE Select	ENSP00000412237.1:p.Arg177Gly
NM_000572.2:c.529C>G	NP_000563.1:p.Arg177Gly
XM_011509506.1:c.529C>G	XP_011507808.1:p.Arg177Gly
NM_000572.3:c.529C>G MANE Select	NP_000563.1:p.Arg177Gly
NM_001382624.1:c.274C>G	NP_001369553.1:p.Arg92Gly
NR_168466.1:n.826C>G
NR_168467.1:n.356C>G