Canonical Allele Identifier: CA422928852

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206941999T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768654T>G , CM000663.2:g.206768654T>G	GRCh38
NC_000001.10:g.206941999T>G , CM000663.1:g.206941999T>G	GRCh37
NC_000001.9:g.205008622T>G	NCBI36
NG_012088.1:g.8841A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1524A>C
ENST00000471071.2:c.264A>C	ENSP00000493073.2:p.Thr88=
ENST00000640756.2:n.329A>C
ENST00000659065.2:c.402A>C	ENSP00000499588.1:p.Thr134=
ENST00000659642.2:c.402A>C	ENSP00000499509.1:p.Thr134=
ENST00000664374.2:c.402A>C	ENSP00000499664.1:p.Thr134=
ENST00000640756.1:n.318A>C
ENST00000659065.1:c.402A>C	ENSP00000499588.1:p.Thr134=
ENST00000659642.1:c.402A>C	ENSP00000499509.1:p.Thr134=
ENST00000664374.1:c.402A>C	ENSP00000499664.1:p.Thr134=
ENST00000423557.1:c.519A>C MANE Select	ENSP00000412237.1:p.Thr173=
NM_000572.2:c.519A>C	NP_000563.1:p.Thr173=
XM_011509506.1:c.519A>C	XP_011507808.1:p.Thr173=
NM_000572.3:c.519A>C MANE Select	NP_000563.1:p.Thr173=
NM_001382624.1:c.264A>C	NP_001369553.1:p.Thr88=
NR_168466.1:n.816A>C
NR_168467.1:n.346A>C