Canonical Allele Identifier: CA344481646

Gene: IL10

Linked Data

• gnomAD v4: 1-206768689-C-T
• MyVariant Identifiers: chr1:g.206942034C>T (hg19) ; chr1:g.206768689C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768689C>T , CM000663.2:g.206768689C>T	GRCh38
NC_000001.10:g.206942034C>T , CM000663.1:g.206942034C>T	GRCh37
NC_000001.9:g.205008657C>T	NCBI36
NG_012088.1:g.8806G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1489G>A
ENST00000471071.2:c.229G>A	ENSP00000493073.2:p.Asp77Asn
ENST00000640756.2:n.294G>A
ENST00000659065.2:c.367G>A	ENSP00000499588.1:p.Asp123Asn
ENST00000659642.2:c.367G>A	ENSP00000499509.1:p.Asp123Asn
ENST00000664374.2:c.367G>A	ENSP00000499664.1:p.Asp123Asn
ENST00000640756.1:n.283G>A
ENST00000659065.1:c.367G>A	ENSP00000499588.1:p.Asp123Asn
ENST00000659642.1:c.367G>A	ENSP00000499509.1:p.Asp123Asn
ENST00000664374.1:c.367G>A	ENSP00000499664.1:p.Asp123Asn
ENST00000423557.1:c.484G>A MANE Select	ENSP00000412237.1:p.Asp162Asn
NM_000572.2:c.484G>A	NP_000563.1:p.Asp162Asn
XM_011509506.1:c.484G>A	XP_011507808.1:p.Asp162Asn
NM_000572.3:c.484G>A MANE Select	NP_000563.1:p.Asp162Asn
NM_001382624.1:c.229G>A	NP_001369553.1:p.Asp77Asn
NR_168466.1:n.781G>A
NR_168467.1:n.311G>A