Canonical Allele Identifier: CA2483125899

Gene: IL10

Linked Data

• dbSNP Id: rs1447641792

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206769069G>T , CM000663.2:g.206769069G>T	GRCh38
NC_000001.10:g.206942414G>T , CM000663.1:g.206942414G>T	GRCh37
NC_000001.9:g.205009037G>T	NCBI36
NG_012088.1:g.8426C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1109C>A
ENST00000471071.2:c.190-341C>A	ENSP00000493073.2:n.190-341C>A
ENST00000640756.2:n.255-341C>A
ENST00000659065.2:c.328-341C>A	ENSP00000499588.1:n.328-341C>A
ENST00000659642.2:c.328-341C>A	ENSP00000499509.1:n.328-341C>A
ENST00000664374.2:c.328-341C>A	ENSP00000499664.1:n.328-341C>A
ENST00000640756.1:n.244-341C>A
ENST00000659065.1:c.328-341C>A	ENSP00000499588.1:n.328-341C>A
ENST00000659642.1:c.328-341C>A	ENSP00000499509.1:n.328-341C>A
ENST00000664374.1:c.328-341C>A	ENSP00000499664.1:n.328-341C>A
ENST00000423557.1:c.445-341C>A MANE Select	ENSP00000412237.1:n.445-341C>A
ENST00000471071.1:n.360-341C>A
NM_000572.2:c.445-341C>A	NP_000563.1:n.445-341C>A
XM_011509506.1:c.445-341C>A	XP_011507808.1:n.445-341C>A
NM_000572.3:c.445-341C>A MANE Select	NP_000563.1:n.445-341C>A
NM_001382624.1:c.190-341C>A	NP_001369553.1:n.190-341C>A
NR_168466.1:n.742-341C>A
NR_168467.1:n.272-341C>A