Canonical Allele Identifier: CA344481615

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206942021T>A (hg19) ; chr1:g.206768676T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768676T>A , CM000663.2:g.206768676T>A	GRCh38
NC_000001.10:g.206942021T>A , CM000663.1:g.206942021T>A	GRCh37
NC_000001.9:g.205008644T>A	NCBI36
NG_012088.1:g.8819A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1502A>T
ENST00000471071.2:c.242A>T	ENSP00000493073.2:p.Asn81Ile
ENST00000640756.2:n.307A>T
ENST00000659065.2:c.380A>T	ENSP00000499588.1:p.Asn127Ile
ENST00000659642.2:c.380A>T	ENSP00000499509.1:p.Asn127Ile
ENST00000664374.2:c.380A>T	ENSP00000499664.1:p.Asn127Ile
ENST00000640756.1:n.296A>T
ENST00000659065.1:c.380A>T	ENSP00000499588.1:p.Asn127Ile
ENST00000659642.1:c.380A>T	ENSP00000499509.1:p.Asn127Ile
ENST00000664374.1:c.380A>T	ENSP00000499664.1:p.Asn127Ile
ENST00000423557.1:c.497A>T MANE Select	ENSP00000412237.1:p.Asn166Ile
NM_000572.2:c.497A>T	NP_000563.1:p.Asn166Ile
XM_011509506.1:c.497A>T	XP_011507808.1:p.Asn166Ile
NM_000572.3:c.497A>T MANE Select	NP_000563.1:p.Asn166Ile
NM_001382624.1:c.242A>T	NP_001369553.1:p.Asn81Ile
NR_168466.1:n.794A>T
NR_168467.1:n.324A>T