Canonical Allele Identifier: CA2650218373

Gene: IL10

Linked Data

• gnomAD v4: 1-206770716-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770716T>C , CM000663.2:g.206770716T>C	GRCh38
NC_000001.10:g.206944061T>C , CM000663.1:g.206944061T>C	GRCh37
NC_000001.9:g.205010684T>C	NCBI36
NG_012088.1:g.6779A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.283+191A>G
ENST00000471071.2:c.123+191A>G	ENSP00000493073.2:n.123+191A>G
ENST00000659065.2:c.261+191A>G	ENSP00000499588.1:n.261+191A>G
ENST00000659642.2:c.261+191A>G	ENSP00000499509.1:n.261+191A>G
ENST00000664374.2:c.261+191A>G	ENSP00000499664.1:n.261+191A>G
ENST00000659065.1:c.261+191A>G	ENSP00000499588.1:n.261+191A>G
ENST00000659642.1:c.261+191A>G	ENSP00000499509.1:n.261+191A>G
ENST00000664374.1:c.261+191A>G	ENSP00000499664.1:n.261+191A>G
ENST00000367099.3:n.283+191A>G
ENST00000423557.1:c.378+191A>G MANE Select	ENSP00000412237.1:n.378+191A>G
ENST00000471071.1:n.293+191A>G
NM_000572.2:c.378+191A>G	NP_000563.1:n.378+191A>G
XM_011509506.1:c.378+191A>G	XP_011507808.1:n.378+191A>G
NM_000572.3:c.378+191A>G MANE Select	NP_000563.1:n.378+191A>G
NM_001382624.1:c.123+191A>G	NP_001369553.1:n.123+191A>G
NR_168466.1:n.437+191A>G