Canonical Allele Identifier: CA344481728

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206942068T>A (hg19) ; chr1:g.206768723T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768723T>A , CM000663.2:g.206768723T>A	GRCh38
NC_000001.10:g.206942068T>A , CM000663.1:g.206942068T>A	GRCh37
NC_000001.9:g.205008691T>A	NCBI36
NG_012088.1:g.8772A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1455A>T
ENST00000471071.2:c.195A>T	ENSP00000493073.2:p.Gln65His
ENST00000640756.2:n.260A>T
ENST00000659065.2:c.333A>T	ENSP00000499588.1:p.Gln111His
ENST00000659642.2:c.333A>T	ENSP00000499509.1:p.Gln111His
ENST00000664374.2:c.333A>T	ENSP00000499664.1:p.Gln111His
ENST00000640756.1:n.249A>T
ENST00000659065.1:c.333A>T	ENSP00000499588.1:p.Gln111His
ENST00000659642.1:c.333A>T	ENSP00000499509.1:p.Gln111His
ENST00000664374.1:c.333A>T	ENSP00000499664.1:p.Gln111His
ENST00000423557.1:c.450A>T MANE Select	ENSP00000412237.1:p.Gln150His
ENST00000471071.1:n.365A>T
NM_000572.2:c.450A>T	NP_000563.1:p.Gln150His
XM_011509506.1:c.450A>T	XP_011507808.1:p.Gln150His
NM_000572.3:c.450A>T MANE Select	NP_000563.1:p.Gln150His
NM_001382624.1:c.195A>T	NP_001369553.1:p.Gln65His
NR_168466.1:n.747A>T
NR_168467.1:n.277A>T