Canonical Allele Identifier: CA422928840

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206941990T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768645T>G , CM000663.2:g.206768645T>G	GRCh38
NC_000001.10:g.206941990T>G , CM000663.1:g.206941990T>G	GRCh37
NC_000001.9:g.205008613T>G	NCBI36
NG_012088.1:g.8850A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1533A>C
ENST00000471071.2:c.273A>C	ENSP00000493073.2:p.Ile91=
ENST00000640756.2:n.338A>C
ENST00000659065.2:c.411A>C	ENSP00000499588.1:p.Ile137=
ENST00000659642.2:c.411A>C	ENSP00000499509.1:p.Ile137=
ENST00000664374.2:c.411A>C	ENSP00000499664.1:p.Ile137=
ENST00000640756.1:n.327A>C
ENST00000659065.1:c.411A>C	ENSP00000499588.1:p.Ile137=
ENST00000659642.1:c.411A>C	ENSP00000499509.1:p.Ile137=
ENST00000664374.1:c.411A>C	ENSP00000499664.1:p.Ile137=
ENST00000423557.1:c.528A>C MANE Select	ENSP00000412237.1:p.Ile176=
NM_000572.2:c.528A>C	NP_000563.1:p.Ile176=
XM_011509506.1:c.528A>C	XP_011507808.1:p.Ile176=
NM_000572.3:c.528A>C MANE Select	NP_000563.1:p.Ile176=
NM_001382624.1:c.273A>C	NP_001369553.1:p.Ile91=
NR_168466.1:n.825A>C
NR_168467.1:n.355A>C