Canonical Allele Identifier: CA344481667

Gene: IL10

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1481G>C
ENST00000471071.2:c.221G>C	ENSP00000493073.2:p.Ser74Thr
ENST00000640756.2:n.286G>C
ENST00000659065.2:c.359G>C	ENSP00000499588.1:p.Ser120Thr
ENST00000659642.2:c.359G>C	ENSP00000499509.1:p.Ser120Thr
ENST00000664374.2:c.359G>C	ENSP00000499664.1:p.Ser120Thr
ENST00000640756.1:n.275G>C
ENST00000659065.1:c.359G>C	ENSP00000499588.1:p.Ser120Thr
ENST00000659642.1:c.359G>C	ENSP00000499509.1:p.Ser120Thr
ENST00000664374.1:c.359G>C	ENSP00000499664.1:p.Ser120Thr
ENST00000423557.1:c.476G>C MANE Select	ENSP00000412237.1:p.Ser159Thr
ENST00000471071.1:n.391G>C
NM_000572.2:c.476G>C	NP_000563.1:p.Ser159Thr
XM_011509506.1:c.476G>C	XP_011507808.1:p.Ser159Thr
NM_000572.3:c.476G>C MANE Select	NP_000563.1:p.Ser159Thr
NM_001382624.1:c.221G>C	NP_001369553.1:p.Ser74Thr
NR_168466.1:n.773G>C
NR_168467.1:n.303G>C