Canonical Allele Identifier: CA528574579

Gene: IL10

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206770368G>T , CM000663.2:g.206770368G>T	GRCh38
NC_000001.10:g.206943713G>T , CM000663.1:g.206943713G>T	GRCh37
NC_000001.9:g.205010336G>T	NCBI36
NG_012088.1:g.7127C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.284-474C>A
ENST00000471071.2:c.124-474C>A	ENSP00000493073.2:n.124-474C>A
ENST00000640756.2:n.188+31C>A
ENST00000659065.2:c.262-474C>A	ENSP00000499588.1:n.262-474C>A
ENST00000659642.2:c.262-474C>A	ENSP00000499509.1:n.262-474C>A
ENST00000664374.2:c.262-474C>A	ENSP00000499664.1:n.262-474C>A
ENST00000640756.1:n.177+31C>A
ENST00000659065.1:c.262-474C>A	ENSP00000499588.1:n.262-474C>A
ENST00000659642.1:c.262-474C>A	ENSP00000499509.1:n.262-474C>A
ENST00000664374.1:c.262-474C>A	ENSP00000499664.1:n.262-474C>A
ENST00000367099.3:n.284-474C>A
ENST00000423557.1:c.379-474C>A MANE Select	ENSP00000412237.1:n.379-474C>A
ENST00000471071.1:n.294-474C>A
NM_000572.2:c.379-474C>A	NP_000563.1:n.379-474C>A
XM_011509506.1:c.379-474C>A	XP_011507808.1:n.379-474C>A
NM_000572.3:c.379-474C>A MANE Select	NP_000563.1:n.379-474C>A
NM_001382624.1:c.124-474C>A	NP_001369553.1:n.124-474C>A
NR_168466.1:n.438-49C>A
NR_168467.1:n.205+31C>A