Canonical Allele Identifier: CA344481562

Gene: IL10

Linked Data

• dbSNP Id: rs1372191956
• gnomAD v4: 1-206768655-G-A
• MyVariant Identifiers: chr1:g.206942000G>A (hg19) ; chr1:g.206768655G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768655G>A , CM000663.2:g.206768655G>A	GRCh38
NC_000001.10:g.206942000G>A , CM000663.1:g.206942000G>A	GRCh37
NC_000001.9:g.205008623G>A	NCBI36
NG_012088.1:g.8840C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1523C>T
ENST00000471071.2:c.263C>T	ENSP00000493073.2:p.Thr88Ile
ENST00000640756.2:n.328C>T
ENST00000659065.2:c.401C>T	ENSP00000499588.1:p.Thr134Ile
ENST00000659642.2:c.401C>T	ENSP00000499509.1:p.Thr134Ile
ENST00000664374.2:c.401C>T	ENSP00000499664.1:p.Thr134Ile
ENST00000640756.1:n.317C>T
ENST00000659065.1:c.401C>T	ENSP00000499588.1:p.Thr134Ile
ENST00000659642.1:c.401C>T	ENSP00000499509.1:p.Thr134Ile
ENST00000664374.1:c.401C>T	ENSP00000499664.1:p.Thr134Ile
ENST00000423557.1:c.518C>T MANE Select	ENSP00000412237.1:p.Thr173Ile
NM_000572.2:c.518C>T	NP_000563.1:p.Thr173Ile
XM_011509506.1:c.518C>T	XP_011507808.1:p.Thr173Ile
NM_000572.3:c.518C>T MANE Select	NP_000563.1:p.Thr173Ile
NM_001382624.1:c.263C>T	NP_001369553.1:p.Thr88Ile
NR_168466.1:n.815C>T
NR_168467.1:n.345C>T