Canonical Allele Identifier: CA2650218386

Gene: IL10

Linked Data

• gnomAD v4: 1-206770756-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770756A>C , CM000663.2:g.206770756A>C	GRCh38
NC_000001.10:g.206944101A>C , CM000663.1:g.206944101A>C	GRCh37
NC_000001.9:g.205010724A>C	NCBI36
NG_012088.1:g.6739T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.283+151T>G
ENST00000471071.2:c.123+151T>G	ENSP00000493073.2:n.123+151T>G
ENST00000659065.2:c.261+151T>G	ENSP00000499588.1:n.261+151T>G
ENST00000659642.2:c.261+151T>G	ENSP00000499509.1:n.261+151T>G
ENST00000664374.2:c.261+151T>G	ENSP00000499664.1:n.261+151T>G
ENST00000659065.1:c.261+151T>G	ENSP00000499588.1:n.261+151T>G
ENST00000659642.1:c.261+151T>G	ENSP00000499509.1:n.261+151T>G
ENST00000664374.1:c.261+151T>G	ENSP00000499664.1:n.261+151T>G
ENST00000367099.3:n.283+151T>G
ENST00000423557.1:c.378+151T>G MANE Select	ENSP00000412237.1:n.378+151T>G
ENST00000471071.1:n.293+151T>G
NM_000572.2:c.378+151T>G	NP_000563.1:n.378+151T>G
XM_011509506.1:c.378+151T>G	XP_011507808.1:n.378+151T>G
NM_000572.3:c.378+151T>G MANE Select	NP_000563.1:n.378+151T>G
NM_001382624.1:c.123+151T>G	NP_001369553.1:n.123+151T>G
NR_168466.1:n.437+151T>G