Canonical Allele Identifier: CA422929002

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206942056G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768711G>A , CM000663.2:g.206768711G>A	GRCh38
NC_000001.10:g.206942056G>A , CM000663.1:g.206942056G>A	GRCh37
NC_000001.9:g.205008679G>A	NCBI36
NG_012088.1:g.8784C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1467C>T
ENST00000471071.2:c.207C>T	ENSP00000493073.2:p.Ile69=
ENST00000640756.2:n.272C>T
ENST00000659065.2:c.345C>T	ENSP00000499588.1:p.Ile115=
ENST00000659642.2:c.345C>T	ENSP00000499509.1:p.Ile115=
ENST00000664374.2:c.345C>T	ENSP00000499664.1:p.Ile115=
ENST00000640756.1:n.261C>T
ENST00000659065.1:c.345C>T	ENSP00000499588.1:p.Ile115=
ENST00000659642.1:c.345C>T	ENSP00000499509.1:p.Ile115=
ENST00000664374.1:c.345C>T	ENSP00000499664.1:p.Ile115=
ENST00000423557.1:c.462C>T MANE Select	ENSP00000412237.1:p.Ile154=
ENST00000471071.1:n.377C>T
NM_000572.2:c.462C>T	NP_000563.1:p.Ile154=
XM_011509506.1:c.462C>T	XP_011507808.1:p.Ile154=
NM_000572.3:c.462C>T MANE Select	NP_000563.1:p.Ile154=
NM_001382624.1:c.207C>T	NP_001369553.1:p.Ile69=
NR_168466.1:n.759C>T
NR_168467.1:n.289C>T