Canonical Allele Identifier: CA344481539

Gene: IL10

Linked Data

• MyVariant Identifiers: chr1:g.206941988C>G (hg19) ; chr1:g.206768643C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768643C>G , CM000663.2:g.206768643C>G	GRCh38
NC_000001.10:g.206941988C>G , CM000663.1:g.206941988C>G	GRCh37
NC_000001.9:g.205008611C>G	NCBI36
NG_012088.1:g.8852G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1535G>C
ENST00000471071.2:c.275G>C	ENSP00000493073.2:p.Arg92Pro
ENST00000640756.2:n.340G>C
ENST00000659065.2:c.413G>C	ENSP00000499588.1:p.Arg138Pro
ENST00000659642.2:c.413G>C	ENSP00000499509.1:p.Arg138Pro
ENST00000664374.2:c.413G>C	ENSP00000499664.1:p.Arg138Pro
ENST00000640756.1:n.329G>C
ENST00000659065.1:c.413G>C	ENSP00000499588.1:p.Arg138Pro
ENST00000659642.1:c.413G>C	ENSP00000499509.1:p.Arg138Pro
ENST00000664374.1:c.413G>C	ENSP00000499664.1:p.Arg138Pro
ENST00000423557.1:c.530G>C MANE Select	ENSP00000412237.1:p.Arg177Pro
NM_000572.2:c.530G>C	NP_000563.1:p.Arg177Pro
XM_011509506.1:c.530G>C	XP_011507808.1:p.Arg177Pro
NM_000572.3:c.530G>C MANE Select	NP_000563.1:p.Arg177Pro
NM_001382624.1:c.275G>C	NP_001369553.1:p.Arg92Pro
NR_168466.1:n.827G>C
NR_168467.1:n.357G>C