Canonical Allele Identifier: CA2483125794
Gene: IL10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206768802A= , CM000663.2:g.206768802A= GRCh38
NC_000001.10:g.206942147A= , CM000663.1:g.206942147A= GRCh37
NC_000001.9:g.205008770A= NCBI36
NG_012088.1:g.8693T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367099.4:n.1376T=
ENST00000471071.2:c.190-74T= ENSP00000493073.2:n.190-74T=
ENST00000640756.2:n.255-74T=
ENST00000659065.2:c.328-74T= ENSP00000499588.1:n.328-74T=
ENST00000659642.2:c.328-74T= ENSP00000499509.1:n.328-74T=
ENST00000664374.2:c.328-74T= ENSP00000499664.1:n.328-74T=
ENST00000640756.1:n.244-74T=
ENST00000659065.1:c.328-74T= ENSP00000499588.1:n.328-74T=
ENST00000659642.1:c.328-74T= ENSP00000499509.1:n.328-74T=
ENST00000664374.1:c.328-74T= ENSP00000499664.1:n.328-74T=
ENST00000423557.1:c.445-74T= MANE Select ENSP00000412237.1:n.445-74T=
ENST00000471071.1:n.360-74T=
NM_000572.2:c.445-74T= NP_000563.1:n.445-74T=
XM_011509506.1:c.445-74T= XP_011507808.1:n.445-74T=
NM_000572.3:c.445-74T= MANE Select NP_000563.1:n.445-74T=
NM_001382624.1:c.190-74T= NP_001369553.1:n.190-74T=
NR_168466.1:n.742-74T=
NR_168467.1:n.272-74T=