Canonical Allele Identifier: CA1363725

Gene: IL10

Linked Data

• ClinVar Variation Id: 1488399
• ClinVar RCV Id: RCV001988560
• dbSNP Id: rs762496248
• ExAC: 1:206941997 A / G
• gnomAD v2: 1-206941997-A-G
• gnomAD v3: 1-206768652-A-G
• gnomAD v4: 1-206768652-A-G
• MyVariant Identifiers: chr1:g.206941997A>G (hg19) ; chr1:g.206768652A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768652A>G , CM000663.2:g.206768652A>G	GRCh38
NC_000001.10:g.206941997A>G , CM000663.1:g.206941997A>G	GRCh37
NC_000001.9:g.205008620A>G	NCBI36
NG_012088.1:g.8843T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1526T>C
ENST00000471071.2:c.266T>C	ENSP00000493073.2:p.Met89Thr
ENST00000640756.2:n.331T>C
ENST00000659065.2:c.404T>C	ENSP00000499588.1:p.Met135Thr
ENST00000659642.2:c.404T>C	ENSP00000499509.1:p.Met135Thr
ENST00000664374.2:c.404T>C	ENSP00000499664.1:p.Met135Thr
ENST00000640756.1:n.320T>C
ENST00000659065.1:c.404T>C	ENSP00000499588.1:p.Met135Thr
ENST00000659642.1:c.404T>C	ENSP00000499509.1:p.Met135Thr
ENST00000664374.1:c.404T>C	ENSP00000499664.1:p.Met135Thr
ENST00000423557.1:c.521T>C MANE Select	ENSP00000412237.1:p.Met174Thr
NM_000572.2:c.521T>C	NP_000563.1:p.Met174Thr
XM_011509506.1:c.521T>C	XP_011507808.1:p.Met174Thr
NM_000572.3:c.521T>C MANE Select	NP_000563.1:p.Met174Thr
NM_001382624.1:c.266T>C	NP_001369553.1:p.Met89Thr
NR_168466.1:n.818T>C
NR_168467.1:n.348T>C