Canonical Allele Identifier: CA422928866

Gene: IL10

Linked Data

• ClinVar Variation Id: 1578342
• ClinVar RCV Id: RCV002090549
• dbSNP Id: rs142093260
• gnomAD v2: 1-206942008-G-A
• gnomAD v4: 1-206768663-G-A
• MyVariant Identifiers: chr1:g.206942008G>A (hg19) ; chr1:g.206768663G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768663G>A , CM000663.2:g.206768663G>A	GRCh38
NC_000001.10:g.206942008G>A , CM000663.1:g.206942008G>A	GRCh37
NC_000001.9:g.205008631G>A	NCBI36
NG_012088.1:g.8832C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1515C>T
ENST00000471071.2:c.255C>T	ENSP00000493073.2:p.Ala85=
ENST00000640756.2:n.320C>T
ENST00000659065.2:c.393C>T	ENSP00000499588.1:p.Ala131=
ENST00000659642.2:c.393C>T	ENSP00000499509.1:p.Ala131=
ENST00000664374.2:c.393C>T	ENSP00000499664.1:p.Ala131=
ENST00000640756.1:n.309C>T
ENST00000659065.1:c.393C>T	ENSP00000499588.1:p.Ala131=
ENST00000659642.1:c.393C>T	ENSP00000499509.1:p.Ala131=
ENST00000664374.1:c.393C>T	ENSP00000499664.1:p.Ala131=
ENST00000423557.1:c.510C>T MANE Select	ENSP00000412237.1:p.Ala170=
NM_000572.2:c.510C>T	NP_000563.1:p.Ala170=
XM_011509506.1:c.510C>T	XP_011507808.1:p.Ala170=
NM_000572.3:c.510C>T MANE Select	NP_000563.1:p.Ala170=
NM_001382624.1:c.255C>T	NP_001369553.1:p.Ala85=
NR_168466.1:n.807C>T
NR_168467.1:n.337C>T