Canonical Allele Identifier: CA344481630

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206942028A>C (hg19) ; chr1:g.206768683A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768683A>C , CM000663.2:g.206768683A>C	GRCh38
NC_000001.10:g.206942028A>C , CM000663.1:g.206942028A>C	GRCh37
NC_000001.9:g.205008651A>C	NCBI36
NG_012088.1:g.8812T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1495T>G
ENST00000471071.2:c.235T>G	ENSP00000493073.2:p.Phe79Val
ENST00000640756.2:n.300T>G
ENST00000659065.2:c.373T>G	ENSP00000499588.1:p.Phe125Val
ENST00000659642.2:c.373T>G	ENSP00000499509.1:p.Phe125Val
ENST00000664374.2:c.373T>G	ENSP00000499664.1:p.Phe125Val
ENST00000640756.1:n.289T>G
ENST00000659065.1:c.373T>G	ENSP00000499588.1:p.Phe125Val
ENST00000659642.1:c.373T>G	ENSP00000499509.1:p.Phe125Val
ENST00000664374.1:c.373T>G	ENSP00000499664.1:p.Phe125Val
ENST00000423557.1:c.490T>G MANE Select	ENSP00000412237.1:p.Phe164Val
NM_000572.2:c.490T>G	NP_000563.1:p.Phe164Val
XM_011509506.1:c.490T>G	XP_011507808.1:p.Phe164Val
NM_000572.3:c.490T>G MANE Select	NP_000563.1:p.Phe164Val
NM_001382624.1:c.235T>G	NP_001369553.1:p.Phe79Val
NR_168466.1:n.787T>G
NR_168467.1:n.317T>G