Canonical Allele Identifier: CA344481620

Gene: IL10

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1499T>G
ENST00000471071.2:c.239T>G	ENSP00000493073.2:p.Ile80Ser
ENST00000640756.2:n.304T>G
ENST00000659065.2:c.377T>G	ENSP00000499588.1:p.Ile126Ser
ENST00000659642.2:c.377T>G	ENSP00000499509.1:p.Ile126Ser
ENST00000664374.2:c.377T>G	ENSP00000499664.1:p.Ile126Ser
ENST00000640756.1:n.293T>G
ENST00000659065.1:c.377T>G	ENSP00000499588.1:p.Ile126Ser
ENST00000659642.1:c.377T>G	ENSP00000499509.1:p.Ile126Ser
ENST00000664374.1:c.377T>G	ENSP00000499664.1:p.Ile126Ser
ENST00000423557.1:c.494T>G MANE Select	ENSP00000412237.1:p.Ile165Ser
NM_000572.2:c.494T>G	NP_000563.1:p.Ile165Ser
XM_011509506.1:c.494T>G	XP_011507808.1:p.Ile165Ser
NM_000572.3:c.494T>G MANE Select	NP_000563.1:p.Ile165Ser
NM_001382624.1:c.239T>G	NP_001369553.1:p.Ile80Ser
NR_168466.1:n.791T>G
NR_168467.1:n.321T>G