Canonical Allele Identifier: CA2650218301

Gene: IL10

Linked Data

• gnomAD v4: 1-206770629-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770629T>G , CM000663.2:g.206770629T>G	GRCh38
NC_000001.10:g.206943974T>G , CM000663.1:g.206943974T>G	GRCh37
NC_000001.9:g.205010597T>G	NCBI36
NG_012088.1:g.6866A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.283+278A>C
ENST00000471071.2:c.123+278A>C	ENSP00000493073.2:n.123+278A>C
ENST00000659065.2:c.261+278A>C	ENSP00000499588.1:n.261+278A>C
ENST00000659642.2:c.261+278A>C	ENSP00000499509.1:n.261+278A>C
ENST00000664374.2:c.261+278A>C	ENSP00000499664.1:n.261+278A>C
ENST00000659065.1:c.261+278A>C	ENSP00000499588.1:n.261+278A>C
ENST00000659642.1:c.261+278A>C	ENSP00000499509.1:n.261+278A>C
ENST00000664374.1:c.261+278A>C	ENSP00000499664.1:n.261+278A>C
ENST00000367099.3:n.283+278A>C
ENST00000423557.1:c.378+278A>C MANE Select	ENSP00000412237.1:n.378+278A>C
ENST00000471071.1:n.293+278A>C
NM_000572.2:c.378+278A>C	NP_000563.1:n.378+278A>C
XM_011509506.1:c.378+278A>C	XP_011507808.1:n.378+278A>C
NM_000572.3:c.378+278A>C MANE Select	NP_000563.1:n.378+278A>C
NM_001382624.1:c.123+278A>C	NP_001369553.1:n.123+278A>C
NR_168466.1:n.437+278A>C