Canonical Allele Identifier: CA344481621

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206942024A>G (hg19) ; chr1:g.206768679A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768679A>G , CM000663.2:g.206768679A>G	GRCh38
NC_000001.10:g.206942024A>G , CM000663.1:g.206942024A>G	GRCh37
NC_000001.9:g.205008647A>G	NCBI36
NG_012088.1:g.8816T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1499T>C
ENST00000471071.2:c.239T>C	ENSP00000493073.2:p.Ile80Thr
ENST00000640756.2:n.304T>C
ENST00000659065.2:c.377T>C	ENSP00000499588.1:p.Ile126Thr
ENST00000659642.2:c.377T>C	ENSP00000499509.1:p.Ile126Thr
ENST00000664374.2:c.377T>C	ENSP00000499664.1:p.Ile126Thr
ENST00000640756.1:n.293T>C
ENST00000659065.1:c.377T>C	ENSP00000499588.1:p.Ile126Thr
ENST00000659642.1:c.377T>C	ENSP00000499509.1:p.Ile126Thr
ENST00000664374.1:c.377T>C	ENSP00000499664.1:p.Ile126Thr
ENST00000423557.1:c.494T>C MANE Select	ENSP00000412237.1:p.Ile165Thr
NM_000572.2:c.494T>C	NP_000563.1:p.Ile165Thr
XM_011509506.1:c.494T>C	XP_011507808.1:p.Ile165Thr
NM_000572.3:c.494T>C MANE Select	NP_000563.1:p.Ile165Thr
NM_001382624.1:c.239T>C	NP_001369553.1:p.Ile80Thr
NR_168466.1:n.791T>C
NR_168467.1:n.321T>C