Canonical Allele Identifier: CA344481560
Gene: IL10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206768653T>C , CM000663.2:g.206768653T>C GRCh38
NC_000001.10:g.206941998T>C , CM000663.1:g.206941998T>C GRCh37
NC_000001.9:g.205008621T>C NCBI36
NG_012088.1:g.8842A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367099.4:n.1525A>G
ENST00000471071.2:c.265A>G ENSP00000493073.2:p.Met89Val
ENST00000640756.2:n.330A>G
ENST00000659065.2:c.403A>G ENSP00000499588.1:p.Met135Val
ENST00000659642.2:c.403A>G ENSP00000499509.1:p.Met135Val
ENST00000664374.2:c.403A>G ENSP00000499664.1:p.Met135Val
ENST00000640756.1:n.319A>G
ENST00000659065.1:c.403A>G ENSP00000499588.1:p.Met135Val
ENST00000659642.1:c.403A>G ENSP00000499509.1:p.Met135Val
ENST00000664374.1:c.403A>G ENSP00000499664.1:p.Met135Val
ENST00000423557.1:c.520A>G MANE Select ENSP00000412237.1:p.Met174Val
NM_000572.2:c.520A>G NP_000563.1:p.Met174Val
XM_011509506.1:c.520A>G XP_011507808.1:p.Met174Val
NM_000572.3:c.520A>G MANE Select NP_000563.1:p.Met174Val
NM_001382624.1:c.265A>G NP_001369553.1:p.Met89Val
NR_168466.1:n.817A>G
NR_168467.1:n.347A>G