Canonical Allele Identifier: CA344481570

Gene: IL10

Linked Data

• gnomAD v4: 1-206768657-C-A
• MyVariant Identifiers: chr1:g.206942002C>A (hg19) ; chr1:g.206768657C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768657C>A , CM000663.2:g.206768657C>A	GRCh38
NC_000001.10:g.206942002C>A , CM000663.1:g.206942002C>A	GRCh37
NC_000001.9:g.205008625C>A	NCBI36
NG_012088.1:g.8838G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1521G>T
ENST00000471071.2:c.261G>T	ENSP00000493073.2:p.Met87Ile
ENST00000640756.2:n.326G>T
ENST00000659065.2:c.399G>T	ENSP00000499588.1:p.Met133Ile
ENST00000659642.2:c.399G>T	ENSP00000499509.1:p.Met133Ile
ENST00000664374.2:c.399G>T	ENSP00000499664.1:p.Met133Ile
ENST00000640756.1:n.315G>T
ENST00000659065.1:c.399G>T	ENSP00000499588.1:p.Met133Ile
ENST00000659642.1:c.399G>T	ENSP00000499509.1:p.Met133Ile
ENST00000664374.1:c.399G>T	ENSP00000499664.1:p.Met133Ile
ENST00000423557.1:c.516G>T MANE Select	ENSP00000412237.1:p.Met172Ile
NM_000572.2:c.516G>T	NP_000563.1:p.Met172Ile
XM_011509506.1:c.516G>T	XP_011507808.1:p.Met172Ile
NM_000572.3:c.516G>T MANE Select	NP_000563.1:p.Met172Ile
NM_001382624.1:c.261G>T	NP_001369553.1:p.Met87Ile
NR_168466.1:n.813G>T
NR_168467.1:n.343G>T