Canonical Allele Identifier: CA344481731

Gene: IL10

Linked Data

• gnomAD v4: 1-206768724-T-C
• MyVariant Identifiers: chr1:g.206942069T>C (hg19) ; chr1:g.206768724T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768724T>C , CM000663.2:g.206768724T>C	GRCh38
NC_000001.10:g.206942069T>C , CM000663.1:g.206942069T>C	GRCh37
NC_000001.9:g.205008692T>C	NCBI36
NG_012088.1:g.8771A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1454A>G
ENST00000471071.2:c.194A>G	ENSP00000493073.2:p.Gln65Arg
ENST00000640756.2:n.259A>G
ENST00000659065.2:c.332A>G	ENSP00000499588.1:p.Gln111Arg
ENST00000659642.2:c.332A>G	ENSP00000499509.1:p.Gln111Arg
ENST00000664374.2:c.332A>G	ENSP00000499664.1:p.Gln111Arg
ENST00000640756.1:n.248A>G
ENST00000659065.1:c.332A>G	ENSP00000499588.1:p.Gln111Arg
ENST00000659642.1:c.332A>G	ENSP00000499509.1:p.Gln111Arg
ENST00000664374.1:c.332A>G	ENSP00000499664.1:p.Gln111Arg
ENST00000423557.1:c.449A>G MANE Select	ENSP00000412237.1:p.Gln150Arg
ENST00000471071.1:n.364A>G
NM_000572.2:c.449A>G	NP_000563.1:p.Gln150Arg
XM_011509506.1:c.449A>G	XP_011507808.1:p.Gln150Arg
NM_000572.3:c.449A>G MANE Select	NP_000563.1:p.Gln150Arg
NM_001382624.1:c.194A>G	NP_001369553.1:p.Gln65Arg
NR_168466.1:n.746A>G
NR_168467.1:n.276A>G