Canonical Allele Identifier: CA2650218385

Gene: IL10

Linked Data

• dbSNP Id: rs2102438830
• gnomAD v4: 1-206770724-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770729dup , CM000663.2:g.206770729dup	GRCh38
NC_000001.10:g.206944074dup , CM000663.1:g.206944074dup	GRCh37
NC_000001.9:g.205010697dup	NCBI36
NG_012088.1:g.6770dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.283+182dup
ENST00000471071.2:c.123+182dup	ENSP00000493073.2:n.123+182dup
ENST00000659065.2:c.261+182dup	ENSP00000499588.1:n.261+182dup
ENST00000659642.2:c.261+182dup	ENSP00000499509.1:n.261+182dup
ENST00000664374.2:c.261+182dup	ENSP00000499664.1:n.261+182dup
ENST00000659065.1:c.261+182dup	ENSP00000499588.1:n.261+182dup
ENST00000659642.1:c.261+182dup	ENSP00000499509.1:n.261+182dup
ENST00000664374.1:c.261+182dup	ENSP00000499664.1:n.261+182dup
ENST00000367099.3:n.283+182dup
ENST00000423557.1:c.378+182dup MANE Select	ENSP00000412237.1:n.378+182dup
ENST00000471071.1:n.293+182dup
NM_000572.2:c.378+182dup	NP_000563.1:n.378+182dup
XM_011509506.1:c.378+182dup	XP_011507808.1:n.378+182dup
NM_000572.3:c.378+182dup MANE Select	NP_000563.1:n.378+182dup
NM_001382624.1:c.123+182dup	NP_001369553.1:n.123+182dup
NR_168466.1:n.437+182dup