Canonical Allele Identifier: CA422928960

Gene: IL10

Linked Data

• ClinVar Variation Id: 2758641
• ClinVar RCV Id: RCV003590190
• dbSNP Id: rs1674735790
• MyVariant Identifiers: chr1:g.206942047G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768702G>A , CM000663.2:g.206768702G>A	GRCh38
NC_000001.10:g.206942047G>A , CM000663.1:g.206942047G>A	GRCh37
NC_000001.9:g.205008670G>A	NCBI36
NG_012088.1:g.8793C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1476C>T
ENST00000471071.2:c.216C>T	ENSP00000493073.2:p.Ala72=
ENST00000640756.2:n.281C>T
ENST00000659065.2:c.354C>T	ENSP00000499588.1:p.Ala118=
ENST00000659642.2:c.354C>T	ENSP00000499509.1:p.Ala118=
ENST00000664374.2:c.354C>T	ENSP00000499664.1:p.Ala118=
ENST00000640756.1:n.270C>T
ENST00000659065.1:c.354C>T	ENSP00000499588.1:p.Ala118=
ENST00000659642.1:c.354C>T	ENSP00000499509.1:p.Ala118=
ENST00000664374.1:c.354C>T	ENSP00000499664.1:p.Ala118=
ENST00000423557.1:c.471C>T MANE Select	ENSP00000412237.1:p.Ala157=
ENST00000471071.1:n.386C>T
NM_000572.2:c.471C>T	NP_000563.1:p.Ala157=
XM_011509506.1:c.471C>T	XP_011507808.1:p.Ala157=
NM_000572.3:c.471C>T MANE Select	NP_000563.1:p.Ala157=
NM_001382624.1:c.216C>T	NP_001369553.1:p.Ala72=
NR_168466.1:n.768C>T
NR_168467.1:n.298C>T