Canonical Allele Identifier: CA2483126504

Gene: IL10

Linked Data

• dbSNP Id: rs1572538821

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770694G>C , CM000663.2:g.206770694G>C	GRCh38
NC_000001.10:g.206944039G>C , CM000663.1:g.206944039G>C	GRCh37
NC_000001.9:g.205010662G>C	NCBI36
NG_012088.1:g.6801C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.283+213C>G
ENST00000471071.2:c.123+213C>G	ENSP00000493073.2:n.123+213C>G
ENST00000659065.2:c.261+213C>G	ENSP00000499588.1:n.261+213C>G
ENST00000659642.2:c.261+213C>G	ENSP00000499509.1:n.261+213C>G
ENST00000664374.2:c.261+213C>G	ENSP00000499664.1:n.261+213C>G
ENST00000659065.1:c.261+213C>G	ENSP00000499588.1:n.261+213C>G
ENST00000659642.1:c.261+213C>G	ENSP00000499509.1:n.261+213C>G
ENST00000664374.1:c.261+213C>G	ENSP00000499664.1:n.261+213C>G
ENST00000367099.3:n.283+213C>G
ENST00000423557.1:c.378+213C>G MANE Select	ENSP00000412237.1:n.378+213C>G
ENST00000471071.1:n.293+213C>G
NM_000572.2:c.378+213C>G	NP_000563.1:n.378+213C>G
XM_011509506.1:c.378+213C>G	XP_011507808.1:n.378+213C>G
NM_000572.3:c.378+213C>G MANE Select	NP_000563.1:n.378+213C>G
NM_001382624.1:c.123+213C>G	NP_001369553.1:n.123+213C>G
NR_168466.1:n.437+213C>G