Canonical Allele Identifier: CA344481675

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206942045A>C (hg19) ; chr1:g.206768700A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768700A>C , CM000663.2:g.206768700A>C	GRCh38
NC_000001.10:g.206942045A>C , CM000663.1:g.206942045A>C	GRCh37
NC_000001.9:g.205008668A>C	NCBI36
NG_012088.1:g.8795T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1478T>G
ENST00000471071.2:c.218T>G	ENSP00000493073.2:p.Met73Arg
ENST00000640756.2:n.283T>G
ENST00000659065.2:c.356T>G	ENSP00000499588.1:p.Met119Arg
ENST00000659642.2:c.356T>G	ENSP00000499509.1:p.Met119Arg
ENST00000664374.2:c.356T>G	ENSP00000499664.1:p.Met119Arg
ENST00000640756.1:n.272T>G
ENST00000659065.1:c.356T>G	ENSP00000499588.1:p.Met119Arg
ENST00000659642.1:c.356T>G	ENSP00000499509.1:p.Met119Arg
ENST00000664374.1:c.356T>G	ENSP00000499664.1:p.Met119Arg
ENST00000423557.1:c.473T>G MANE Select	ENSP00000412237.1:p.Met158Arg
ENST00000471071.1:n.388T>G
NM_000572.2:c.473T>G	NP_000563.1:p.Met158Arg
XM_011509506.1:c.473T>G	XP_011507808.1:p.Met158Arg
NM_000572.3:c.473T>G MANE Select	NP_000563.1:p.Met158Arg
NM_001382624.1:c.218T>G	NP_001369553.1:p.Met73Arg
NR_168466.1:n.770T>G
NR_168467.1:n.300T>G