Canonical Allele Identifier: CA730536567

Gene: IL10

Linked Data

• dbSNP Id: rs1316220046
• gnomAD v3: 1-206769028-T-C
• gnomAD v4: 1-206769028-T-C
• MyVariant Identifiers: chr1:g.206942373T>C (hg19) ; chr1:g.206769028T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206769028T>C , CM000663.2:g.206769028T>C	GRCh38
NC_000001.10:g.206942373T>C , CM000663.1:g.206942373T>C	GRCh37
NC_000001.9:g.205008996T>C	NCBI36
NG_012088.1:g.8467A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367099.4:n.1150A>G
ENST00000471071.2:c.190-300A>G	ENSP00000493073.2:n.190-300A>G
ENST00000640756.2:n.255-300A>G
ENST00000659065.2:c.328-300A>G	ENSP00000499588.1:n.328-300A>G
ENST00000659642.2:c.328-300A>G	ENSP00000499509.1:n.328-300A>G
ENST00000664374.2:c.328-300A>G	ENSP00000499664.1:n.328-300A>G
ENST00000640756.1:n.244-300A>G
ENST00000659065.1:c.328-300A>G	ENSP00000499588.1:n.328-300A>G
ENST00000659642.1:c.328-300A>G	ENSP00000499509.1:n.328-300A>G
ENST00000664374.1:c.328-300A>G	ENSP00000499664.1:n.328-300A>G
ENST00000423557.1:c.445-300A>G MANE Select	ENSP00000412237.1:n.445-300A>G
ENST00000471071.1:n.360-300A>G
NM_000572.2:c.445-300A>G	NP_000563.1:n.445-300A>G
XM_011509506.1:c.445-300A>G	XP_011507808.1:n.445-300A>G
NM_000572.3:c.445-300A>G MANE Select	NP_000563.1:n.445-300A>G
NM_001382624.1:c.190-300A>G	NP_001369553.1:n.190-300A>G
NR_168466.1:n.742-300A>G
NR_168467.1:n.272-300A>G