Canonical Allele Identifier: CA344481610

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206942019A>T (hg19) ; chr1:g.206768674A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768674A>T , CM000663.2:g.206768674A>T	GRCh38
NC_000001.10:g.206942019A>T , CM000663.1:g.206942019A>T	GRCh37
NC_000001.9:g.205008642A>T	NCBI36
NG_012088.1:g.8821T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1504T>A
ENST00000471071.2:c.244T>A	ENSP00000493073.2:p.Tyr82Asn
ENST00000640756.2:n.309T>A
ENST00000659065.2:c.382T>A	ENSP00000499588.1:p.Tyr128Asn
ENST00000659642.2:c.382T>A	ENSP00000499509.1:p.Tyr128Asn
ENST00000664374.2:c.382T>A	ENSP00000499664.1:p.Tyr128Asn
ENST00000640756.1:n.298T>A
ENST00000659065.1:c.382T>A	ENSP00000499588.1:p.Tyr128Asn
ENST00000659642.1:c.382T>A	ENSP00000499509.1:p.Tyr128Asn
ENST00000664374.1:c.382T>A	ENSP00000499664.1:p.Tyr128Asn
ENST00000423557.1:c.499T>A MANE Select	ENSP00000412237.1:p.Tyr167Asn
NM_000572.2:c.499T>A	NP_000563.1:p.Tyr167Asn
XM_011509506.1:c.499T>A	XP_011507808.1:p.Tyr167Asn
NM_000572.3:c.499T>A MANE Select	NP_000563.1:p.Tyr167Asn
NM_001382624.1:c.244T>A	NP_001369553.1:p.Tyr82Asn
NR_168466.1:n.796T>A
NR_168467.1:n.326T>A