Canonical Allele Identifier: CA422928859

Gene: IL10

Linked Data

• ClinVar Variation Id: 795622
• ClinVar RCV Id: RCV001446247
• dbSNP Id: rs1572537757
• MyVariant Identifiers: chr1:g.206942005G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768660G>A , CM000663.2:g.206768660G>A	GRCh38
NC_000001.10:g.206942005G>A , CM000663.1:g.206942005G>A	GRCh37
NC_000001.9:g.205008628G>A	NCBI36
NG_012088.1:g.8835C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1518C>T
ENST00000471071.2:c.258C>T	ENSP00000493073.2:p.Tyr86=
ENST00000640756.2:n.323C>T
ENST00000659065.2:c.396C>T	ENSP00000499588.1:p.Tyr132=
ENST00000659642.2:c.396C>T	ENSP00000499509.1:p.Tyr132=
ENST00000664374.2:c.396C>T	ENSP00000499664.1:p.Tyr132=
ENST00000640756.1:n.312C>T
ENST00000659065.1:c.396C>T	ENSP00000499588.1:p.Tyr132=
ENST00000659642.1:c.396C>T	ENSP00000499509.1:p.Tyr132=
ENST00000664374.1:c.396C>T	ENSP00000499664.1:p.Tyr132=
ENST00000423557.1:c.513C>T MANE Select	ENSP00000412237.1:p.Tyr171=
NM_000572.2:c.513C>T	NP_000563.1:p.Tyr171=
XM_011509506.1:c.513C>T	XP_011507808.1:p.Tyr171=
NM_000572.3:c.513C>T MANE Select	NP_000563.1:p.Tyr171=
NM_001382624.1:c.258C>T	NP_001369553.1:p.Tyr86=
NR_168466.1:n.810C>T
NR_168467.1:n.340C>T