Canonical Allele Identifier: CA422929003

Gene: IL10

Linked Data

• gnomAD v4: 1-206768711-G-T
• MyVariant Identifiers: chr1:g.206942056G>T (hg19)

Genomic Alleles

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

Transcript Alleles

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