Canonical Allele Identifier: CA2650217503

Gene: IL10

Linked Data

• gnomAD v4: 1-206768796-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768796A>C , CM000663.2:g.206768796A>C	GRCh38
NC_000001.10:g.206942141A>C , CM000663.1:g.206942141A>C	GRCh37
NC_000001.9:g.205008764A>C	NCBI36
NG_012088.1:g.8699T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1382T>G
ENST00000471071.2:c.190-68T>G	ENSP00000493073.2:n.190-68T>G
ENST00000640756.2:n.255-68T>G
ENST00000659065.2:c.328-68T>G	ENSP00000499588.1:n.328-68T>G
ENST00000659642.2:c.328-68T>G	ENSP00000499509.1:n.328-68T>G
ENST00000664374.2:c.328-68T>G	ENSP00000499664.1:n.328-68T>G
ENST00000640756.1:n.244-68T>G
ENST00000659065.1:c.328-68T>G	ENSP00000499588.1:n.328-68T>G
ENST00000659642.1:c.328-68T>G	ENSP00000499509.1:n.328-68T>G
ENST00000664374.1:c.328-68T>G	ENSP00000499664.1:n.328-68T>G
ENST00000423557.1:c.445-68T>G MANE Select	ENSP00000412237.1:n.445-68T>G
ENST00000471071.1:n.360-68T>G
NM_000572.2:c.445-68T>G	NP_000563.1:n.445-68T>G
XM_011509506.1:c.445-68T>G	XP_011507808.1:n.445-68T>G
NM_000572.3:c.445-68T>G MANE Select	NP_000563.1:n.445-68T>G
NM_001382624.1:c.190-68T>G	NP_001369553.1:n.190-68T>G
NR_168466.1:n.742-68T>G
NR_168467.1:n.272-68T>G