Canonical Allele Identifier: CA344481696

Gene: IL10

Linked Data

• gnomAD v4: 1-206768708-G-T
• MyVariant Identifiers: chr1:g.206942053G>T (hg19) ; chr1:g.206768708G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768708G>T , CM000663.2:g.206768708G>T	GRCh38
NC_000001.10:g.206942053G>T , CM000663.1:g.206942053G>T	GRCh37
NC_000001.9:g.205008676G>T	NCBI36
NG_012088.1:g.8787C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1470C>A
ENST00000471071.2:c.210C>A	ENSP00000493073.2:p.Tyr70Ter
ENST00000640756.2:n.275C>A
ENST00000659065.2:c.348C>A	ENSP00000499588.1:p.Tyr116Ter
ENST00000659642.2:c.348C>A	ENSP00000499509.1:p.Tyr116Ter
ENST00000664374.2:c.348C>A	ENSP00000499664.1:p.Tyr116Ter
ENST00000640756.1:n.264C>A
ENST00000659065.1:c.348C>A	ENSP00000499588.1:p.Tyr116Ter
ENST00000659642.1:c.348C>A	ENSP00000499509.1:p.Tyr116Ter
ENST00000664374.1:c.348C>A	ENSP00000499664.1:p.Tyr116Ter
ENST00000423557.1:c.465C>A MANE Select	ENSP00000412237.1:p.Tyr155Ter
ENST00000471071.1:n.380C>A
NM_000572.2:c.465C>A	NP_000563.1:p.Tyr155Ter
XM_011509506.1:c.465C>A	XP_011507808.1:p.Tyr155Ter
NM_000572.3:c.465C>A MANE Select	NP_000563.1:p.Tyr155Ter
NM_001382624.1:c.210C>A	NP_001369553.1:p.Tyr70Ter
NR_168466.1:n.762C>A
NR_168467.1:n.292C>A