Canonical Allele Identifier: CA422928915

Gene: IL10

Linked Data

• dbSNP Id: rs2102436716
• gnomAD v4: 1-206768687-G-A
• MyVariant Identifiers: chr1:g.206942032G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768687G>A , CM000663.2:g.206768687G>A	GRCh38
NC_000001.10:g.206942032G>A , CM000663.1:g.206942032G>A	GRCh37
NC_000001.9:g.205008655G>A	NCBI36
NG_012088.1:g.8808C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1491C>T
ENST00000471071.2:c.231C>T	ENSP00000493073.2:p.Asp77=
ENST00000640756.2:n.296C>T
ENST00000659065.2:c.369C>T	ENSP00000499588.1:p.Asp123=
ENST00000659642.2:c.369C>T	ENSP00000499509.1:p.Asp123=
ENST00000664374.2:c.369C>T	ENSP00000499664.1:p.Asp123=
ENST00000640756.1:n.285C>T
ENST00000659065.1:c.369C>T	ENSP00000499588.1:p.Asp123=
ENST00000659642.1:c.369C>T	ENSP00000499509.1:p.Asp123=
ENST00000664374.1:c.369C>T	ENSP00000499664.1:p.Asp123=
ENST00000423557.1:c.486C>T MANE Select	ENSP00000412237.1:p.Asp162=
NM_000572.2:c.486C>T	NP_000563.1:p.Asp162=
XM_011509506.1:c.486C>T	XP_011507808.1:p.Asp162=
NM_000572.3:c.486C>T MANE Select	NP_000563.1:p.Asp162=
NM_001382624.1:c.231C>T	NP_001369553.1:p.Asp77=
NR_168466.1:n.783C>T
NR_168467.1:n.313C>T