Canonical Allele Identifier: CA344481645

Gene: IL10

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1489G>T
ENST00000471071.2:c.229G>T	ENSP00000493073.2:p.Asp77Tyr
ENST00000640756.2:n.294G>T
ENST00000659065.2:c.367G>T	ENSP00000499588.1:p.Asp123Tyr
ENST00000659642.2:c.367G>T	ENSP00000499509.1:p.Asp123Tyr
ENST00000664374.2:c.367G>T	ENSP00000499664.1:p.Asp123Tyr
ENST00000640756.1:n.283G>T
ENST00000659065.1:c.367G>T	ENSP00000499588.1:p.Asp123Tyr
ENST00000659642.1:c.367G>T	ENSP00000499509.1:p.Asp123Tyr
ENST00000664374.1:c.367G>T	ENSP00000499664.1:p.Asp123Tyr
ENST00000423557.1:c.484G>T MANE Select	ENSP00000412237.1:p.Asp162Tyr
NM_000572.2:c.484G>T	NP_000563.1:p.Asp162Tyr
XM_011509506.1:c.484G>T	XP_011507808.1:p.Asp162Tyr
NM_000572.3:c.484G>T MANE Select	NP_000563.1:p.Asp162Tyr
NM_001382624.1:c.229G>T	NP_001369553.1:p.Asp77Tyr
NR_168466.1:n.781G>T
NR_168467.1:n.311G>T