Canonical Allele Identifier: CA344481606

Gene: IL10

Linked Data

• dbSNP Id: rs1674735459
• COSMIC: COSM3943389
• MyVariant Identifiers: chr1:g.206942018T>C (hg19) ; chr1:g.206768673T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768673T>C , CM000663.2:g.206768673T>C	GRCh38
NC_000001.10:g.206942018T>C , CM000663.1:g.206942018T>C	GRCh37
NC_000001.9:g.205008641T>C	NCBI36
NG_012088.1:g.8822A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1505A>G
ENST00000471071.2:c.245A>G	ENSP00000493073.2:p.Tyr82Cys
ENST00000640756.2:n.310A>G
ENST00000659065.2:c.383A>G	ENSP00000499588.1:p.Tyr128Cys
ENST00000659642.2:c.383A>G	ENSP00000499509.1:p.Tyr128Cys
ENST00000664374.2:c.383A>G	ENSP00000499664.1:p.Tyr128Cys
ENST00000640756.1:n.299A>G
ENST00000659065.1:c.383A>G	ENSP00000499588.1:p.Tyr128Cys
ENST00000659642.1:c.383A>G	ENSP00000499509.1:p.Tyr128Cys
ENST00000664374.1:c.383A>G	ENSP00000499664.1:p.Tyr128Cys
ENST00000423557.1:c.500A>G MANE Select	ENSP00000412237.1:p.Tyr167Cys
NM_000572.2:c.500A>G	NP_000563.1:p.Tyr167Cys
XM_011509506.1:c.500A>G	XP_011507808.1:p.Tyr167Cys
NM_000572.3:c.500A>G MANE Select	NP_000563.1:p.Tyr167Cys
NM_001382624.1:c.245A>G	NP_001369553.1:p.Tyr82Cys
NR_168466.1:n.797A>G
NR_168467.1:n.327A>G