Canonical Allele Identifier: CA2650217444

Gene: IL10

Linked Data

• ClinVar Variation Id: 2796283
• ClinVar RCV Id: RCV003753902
• gnomAD v4: 1-206768736-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768736G>A , CM000663.2:g.206768736G>A	GRCh38
NC_000001.10:g.206942081G>A , CM000663.1:g.206942081G>A	GRCh37
NC_000001.9:g.205008704G>A	NCBI36
NG_012088.1:g.8759C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1442C>T
ENST00000471071.2:c.190-8C>T	ENSP00000493073.2:n.190-8C>T
ENST00000640756.2:n.255-8C>T
ENST00000659065.2:c.328-8C>T	ENSP00000499588.1:n.328-8C>T
ENST00000659642.2:c.328-8C>T	ENSP00000499509.1:n.328-8C>T
ENST00000664374.2:c.328-8C>T	ENSP00000499664.1:n.328-8C>T
ENST00000640756.1:n.244-8C>T
ENST00000659065.1:c.328-8C>T	ENSP00000499588.1:n.328-8C>T
ENST00000659642.1:c.328-8C>T	ENSP00000499509.1:n.328-8C>T
ENST00000664374.1:c.328-8C>T	ENSP00000499664.1:n.328-8C>T
ENST00000423557.1:c.445-8C>T MANE Select	ENSP00000412237.1:n.445-8C>T
ENST00000471071.1:n.360-8C>T
NM_000572.2:c.445-8C>T	NP_000563.1:n.445-8C>T
XM_011509506.1:c.445-8C>T	XP_011507808.1:n.445-8C>T
NM_000572.3:c.445-8C>T MANE Select	NP_000563.1:n.445-8C>T
NM_001382624.1:c.190-8C>T	NP_001369553.1:n.190-8C>T
NR_168466.1:n.742-8C>T
NR_168467.1:n.272-8C>T