Canonical Allele Identifier: CA2650218372

Gene: IL10

Linked Data

• gnomAD v4: 1-206770715-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770715C>T , CM000663.2:g.206770715C>T	GRCh38
NC_000001.10:g.206944060C>T , CM000663.1:g.206944060C>T	GRCh37
NC_000001.9:g.205010683C>T	NCBI36
NG_012088.1:g.6780G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.283+192G>A
ENST00000471071.2:c.123+192G>A	ENSP00000493073.2:n.123+192G>A
ENST00000659065.2:c.261+192G>A	ENSP00000499588.1:n.261+192G>A
ENST00000659642.2:c.261+192G>A	ENSP00000499509.1:n.261+192G>A
ENST00000664374.2:c.261+192G>A	ENSP00000499664.1:n.261+192G>A
ENST00000659065.1:c.261+192G>A	ENSP00000499588.1:n.261+192G>A
ENST00000659642.1:c.261+192G>A	ENSP00000499509.1:n.261+192G>A
ENST00000664374.1:c.261+192G>A	ENSP00000499664.1:n.261+192G>A
ENST00000367099.3:n.283+192G>A
ENST00000423557.1:c.378+192G>A MANE Select	ENSP00000412237.1:n.378+192G>A
ENST00000471071.1:n.293+192G>A
NM_000572.2:c.378+192G>A	NP_000563.1:n.378+192G>A
XM_011509506.1:c.378+192G>A	XP_011507808.1:n.378+192G>A
NM_000572.3:c.378+192G>A MANE Select	NP_000563.1:n.378+192G>A
NM_001382624.1:c.123+192G>A	NP_001369553.1:n.123+192G>A
NR_168466.1:n.437+192G>A