Canonical Allele Identifier: CA344481668

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206942042C>T (hg19) ; chr1:g.206768697C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768697C>T , CM000663.2:g.206768697C>T	GRCh38
NC_000001.10:g.206942042C>T , CM000663.1:g.206942042C>T	GRCh37
NC_000001.9:g.205008665C>T	NCBI36
NG_012088.1:g.8798G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1481G>A
ENST00000471071.2:c.221G>A	ENSP00000493073.2:p.Ser74Asn
ENST00000640756.2:n.286G>A
ENST00000659065.2:c.359G>A	ENSP00000499588.1:p.Ser120Asn
ENST00000659642.2:c.359G>A	ENSP00000499509.1:p.Ser120Asn
ENST00000664374.2:c.359G>A	ENSP00000499664.1:p.Ser120Asn
ENST00000640756.1:n.275G>A
ENST00000659065.1:c.359G>A	ENSP00000499588.1:p.Ser120Asn
ENST00000659642.1:c.359G>A	ENSP00000499509.1:p.Ser120Asn
ENST00000664374.1:c.359G>A	ENSP00000499664.1:p.Ser120Asn
ENST00000423557.1:c.476G>A MANE Select	ENSP00000412237.1:p.Ser159Asn
ENST00000471071.1:n.391G>A
NM_000572.2:c.476G>A	NP_000563.1:p.Ser159Asn
XM_011509506.1:c.476G>A	XP_011507808.1:p.Ser159Asn
NM_000572.3:c.476G>A MANE Select	NP_000563.1:p.Ser159Asn
NM_001382624.1:c.221G>A	NP_001369553.1:p.Ser74Asn
NR_168466.1:n.773G>A
NR_168467.1:n.303G>A