Canonical Allele Identifier: CA36549075

Gene: IL10

Linked Data

• dbSNP Id: rs187648997
• gnomAD v3: 1-206770705-A-T
• gnomAD v4: 1-206770705-A-T
• MyVariant Identifiers: chr1:g.206944050A>T (hg19) ; chr1:g.206770705A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770705A>T , CM000663.2:g.206770705A>T	GRCh38
NC_000001.10:g.206944050A>T , CM000663.1:g.206944050A>T	GRCh37
NC_000001.9:g.205010673A>T	NCBI36
NG_012088.1:g.6790T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.283+202T>A
ENST00000471071.2:c.123+202T>A	ENSP00000493073.2:n.123+202T>A
ENST00000659065.2:c.261+202T>A	ENSP00000499588.1:n.261+202T>A
ENST00000659642.2:c.261+202T>A	ENSP00000499509.1:n.261+202T>A
ENST00000664374.2:c.261+202T>A	ENSP00000499664.1:n.261+202T>A
ENST00000659065.1:c.261+202T>A	ENSP00000499588.1:n.261+202T>A
ENST00000659642.1:c.261+202T>A	ENSP00000499509.1:n.261+202T>A
ENST00000664374.1:c.261+202T>A	ENSP00000499664.1:n.261+202T>A
ENST00000367099.3:n.283+202T>A
ENST00000423557.1:c.378+202T>A MANE Select	ENSP00000412237.1:n.378+202T>A
ENST00000471071.1:n.293+202T>A
NM_000572.2:c.378+202T>A	NP_000563.1:n.378+202T>A
XM_011509506.1:c.378+202T>A	XP_011507808.1:n.378+202T>A
NM_000572.3:c.378+202T>A MANE Select	NP_000563.1:n.378+202T>A
NM_001382624.1:c.123+202T>A	NP_001369553.1:n.123+202T>A
NR_168466.1:n.437+202T>A