Canonical Allele Identifier: CA344481739

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206942073G>C (hg19) ; chr1:g.206768728G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768728G>C , CM000663.2:g.206768728G>C	GRCh38
NC_000001.10:g.206942073G>C , CM000663.1:g.206942073G>C	GRCh37
NC_000001.9:g.205008696G>C	NCBI36
NG_012088.1:g.8767C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1450C>G
ENST00000471071.2:c.190C>G	ENSP00000493073.2:p.Leu64Val
ENST00000640756.2:n.255C>G
ENST00000659065.2:c.328C>G	ENSP00000499588.1:p.Leu110Val
ENST00000659642.2:c.328C>G	ENSP00000499509.1:p.Leu110Val
ENST00000664374.2:c.328C>G	ENSP00000499664.1:p.Leu110Val
ENST00000640756.1:n.244C>G
ENST00000659065.1:c.328C>G	ENSP00000499588.1:p.Leu110Val
ENST00000659642.1:c.328C>G	ENSP00000499509.1:p.Leu110Val
ENST00000664374.1:c.328C>G	ENSP00000499664.1:p.Leu110Val
ENST00000423557.1:c.445C>G MANE Select	ENSP00000412237.1:p.Leu149Val
ENST00000471071.1:n.360C>G
NM_000572.2:c.445C>G	NP_000563.1:p.Leu149Val
XM_011509506.1:c.445C>G	XP_011507808.1:p.Leu149Val
NM_000572.3:c.445C>G MANE Select	NP_000563.1:p.Leu149Val
NM_001382624.1:c.190C>G	NP_001369553.1:p.Leu64Val
NR_168466.1:n.742C>G
NR_168467.1:n.272C>G