Canonical Allele Identifier: CA344481617

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206942022T>C (hg19) ; chr1:g.206768677T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768677T>C , CM000663.2:g.206768677T>C	GRCh38
NC_000001.10:g.206942022T>C , CM000663.1:g.206942022T>C	GRCh37
NC_000001.9:g.205008645T>C	NCBI36
NG_012088.1:g.8818A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1501A>G
ENST00000471071.2:c.241A>G	ENSP00000493073.2:p.Asn81Asp
ENST00000640756.2:n.306A>G
ENST00000659065.2:c.379A>G	ENSP00000499588.1:p.Asn127Asp
ENST00000659642.2:c.379A>G	ENSP00000499509.1:p.Asn127Asp
ENST00000664374.2:c.379A>G	ENSP00000499664.1:p.Asn127Asp
ENST00000640756.1:n.295A>G
ENST00000659065.1:c.379A>G	ENSP00000499588.1:p.Asn127Asp
ENST00000659642.1:c.379A>G	ENSP00000499509.1:p.Asn127Asp
ENST00000664374.1:c.379A>G	ENSP00000499664.1:p.Asn127Asp
ENST00000423557.1:c.496A>G MANE Select	ENSP00000412237.1:p.Asn166Asp
NM_000572.2:c.496A>G	NP_000563.1:p.Asn166Asp
XM_011509506.1:c.496A>G	XP_011507808.1:p.Asn166Asp
NM_000572.3:c.496A>G MANE Select	NP_000563.1:p.Asn166Asp
NM_001382624.1:c.241A>G	NP_001369553.1:p.Asn81Asp
NR_168466.1:n.793A>G
NR_168467.1:n.323A>G