Canonical Allele Identifier: CA36548035

Gene: IL10

Linked Data

• dbSNP Id: rs958329254
• MyVariant Identifiers: chr1:g.206942322C>T (hg19) ; chr1:g.206768977C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768977C>T , CM000663.2:g.206768977C>T	GRCh38
NC_000001.10:g.206942322C>T , CM000663.1:g.206942322C>T	GRCh37
NC_000001.9:g.205008945C>T	NCBI36
NG_012088.1:g.8518G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.1201G>A
ENST00000471071.2:c.190-249G>A	ENSP00000493073.2:n.190-249G>A
ENST00000640756.2:n.255-249G>A
ENST00000659065.2:c.328-249G>A	ENSP00000499588.1:n.328-249G>A
ENST00000659642.2:c.328-249G>A	ENSP00000499509.1:n.328-249G>A
ENST00000664374.2:c.328-249G>A	ENSP00000499664.1:n.328-249G>A
ENST00000640756.1:n.244-249G>A
ENST00000659065.1:c.328-249G>A	ENSP00000499588.1:n.328-249G>A
ENST00000659642.1:c.328-249G>A	ENSP00000499509.1:n.328-249G>A
ENST00000664374.1:c.328-249G>A	ENSP00000499664.1:n.328-249G>A
ENST00000423557.1:c.445-249G>A MANE Select	ENSP00000412237.1:n.445-249G>A
ENST00000471071.1:n.360-249G>A
NM_000572.2:c.445-249G>A	NP_000563.1:n.445-249G>A
XM_011509506.1:c.445-249G>A	XP_011507808.1:n.445-249G>A
NM_000572.3:c.445-249G>A MANE Select	NP_000563.1:n.445-249G>A
NM_001382624.1:c.190-249G>A	NP_001369553.1:n.190-249G>A
NR_168466.1:n.742-249G>A
NR_168467.1:n.272-249G>A