Canonical Allele Identifier: CA2483125901

Gene: IL10

Linked Data

• dbSNP Id: rs1674745424

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206769072G>A , CM000663.2:g.206769072G>A	GRCh38
NC_000001.10:g.206942417G>A , CM000663.1:g.206942417G>A	GRCh37
NC_000001.9:g.205009040G>A	NCBI36
NG_012088.1:g.8423C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1106C>T
ENST00000471071.2:c.190-344C>T	ENSP00000493073.2:n.190-344C>T
ENST00000640756.2:n.255-344C>T
ENST00000659065.2:c.328-344C>T	ENSP00000499588.1:n.328-344C>T
ENST00000659642.2:c.328-344C>T	ENSP00000499509.1:n.328-344C>T
ENST00000664374.2:c.328-344C>T	ENSP00000499664.1:n.328-344C>T
ENST00000640756.1:n.244-344C>T
ENST00000659065.1:c.328-344C>T	ENSP00000499588.1:n.328-344C>T
ENST00000659642.1:c.328-344C>T	ENSP00000499509.1:n.328-344C>T
ENST00000664374.1:c.328-344C>T	ENSP00000499664.1:n.328-344C>T
ENST00000423557.1:c.445-344C>T MANE Select	ENSP00000412237.1:n.445-344C>T
ENST00000471071.1:n.360-344C>T
NM_000572.2:c.445-344C>T	NP_000563.1:n.445-344C>T
XM_011509506.1:c.445-344C>T	XP_011507808.1:n.445-344C>T
NM_000572.3:c.445-344C>T MANE Select	NP_000563.1:n.445-344C>T
NM_001382624.1:c.190-344C>T	NP_001369553.1:n.190-344C>T
NR_168466.1:n.742-344C>T
NR_168467.1:n.272-344C>T