Canonical Allele Identifier: CA1363728

Gene: IL10

Linked Data

• dbSNP Id: rs761398096
• ExAC: 1:206942025 T / C
• gnomAD v2: 1-206942025-T-C
• gnomAD v4: 1-206768680-T-C
• MyVariant Identifiers: chr1:g.206942025T>C (hg19) ; chr1:g.206768680T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768680T>C , CM000663.2:g.206768680T>C	GRCh38
NC_000001.10:g.206942025T>C , CM000663.1:g.206942025T>C	GRCh37
NC_000001.9:g.205008648T>C	NCBI36
NG_012088.1:g.8815A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1498A>G
ENST00000471071.2:c.238A>G	ENSP00000493073.2:p.Ile80Val
ENST00000640756.2:n.303A>G
ENST00000659065.2:c.376A>G	ENSP00000499588.1:p.Ile126Val
ENST00000659642.2:c.376A>G	ENSP00000499509.1:p.Ile126Val
ENST00000664374.2:c.376A>G	ENSP00000499664.1:p.Ile126Val
ENST00000640756.1:n.292A>G
ENST00000659065.1:c.376A>G	ENSP00000499588.1:p.Ile126Val
ENST00000659642.1:c.376A>G	ENSP00000499509.1:p.Ile126Val
ENST00000664374.1:c.376A>G	ENSP00000499664.1:p.Ile126Val
ENST00000423557.1:c.493A>G MANE Select	ENSP00000412237.1:p.Ile165Val
NM_000572.2:c.493A>G	NP_000563.1:p.Ile165Val
XM_011509506.1:c.493A>G	XP_011507808.1:p.Ile165Val
NM_000572.3:c.493A>G MANE Select	NP_000563.1:p.Ile165Val
NM_001382624.1:c.238A>G	NP_001369553.1:p.Ile80Val
NR_168466.1:n.790A>G
NR_168467.1:n.320A>G