Canonical Allele Identifier: CA422929064

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206942068T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768723T>C , CM000663.2:g.206768723T>C	GRCh38
NC_000001.10:g.206942068T>C , CM000663.1:g.206942068T>C	GRCh37
NC_000001.9:g.205008691T>C	NCBI36
NG_012088.1:g.8772A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1455A>G
ENST00000471071.2:c.195A>G	ENSP00000493073.2:p.Gln65=
ENST00000640756.2:n.260A>G
ENST00000659065.2:c.333A>G	ENSP00000499588.1:p.Gln111=
ENST00000659642.2:c.333A>G	ENSP00000499509.1:p.Gln111=
ENST00000664374.2:c.333A>G	ENSP00000499664.1:p.Gln111=
ENST00000640756.1:n.249A>G
ENST00000659065.1:c.333A>G	ENSP00000499588.1:p.Gln111=
ENST00000659642.1:c.333A>G	ENSP00000499509.1:p.Gln111=
ENST00000664374.1:c.333A>G	ENSP00000499664.1:p.Gln111=
ENST00000423557.1:c.450A>G MANE Select	ENSP00000412237.1:p.Gln150=
ENST00000471071.1:n.365A>G
NM_000572.2:c.450A>G	NP_000563.1:p.Gln150=
XM_011509506.1:c.450A>G	XP_011507808.1:p.Gln150=
NM_000572.3:c.450A>G MANE Select	NP_000563.1:p.Gln150=
NM_001382624.1:c.195A>G	NP_001369553.1:p.Gln65=
NR_168466.1:n.747A>G
NR_168467.1:n.277A>G