Canonical Allele Identifier: CA1363727

Gene: IL10

Linked Data

• ClinVar Variation Id: 939398
• ClinVar RCV Id: RCV001208795
• dbSNP Id: rs568879359
• ExAC: 1:206942011 T / G
• gnomAD v2: 1-206942011-T-G
• gnomAD v3: 1-206768666-T-G
• gnomAD v4: 1-206768666-T-G
• MyVariant Identifiers: chr1:g.206942011T>G (hg19) ; chr1:g.206768666T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768666T>G , CM000663.2:g.206768666T>G	GRCh38
NC_000001.10:g.206942011T>G , CM000663.1:g.206942011T>G	GRCh37
NC_000001.9:g.205008634T>G	NCBI36
NG_012088.1:g.8829A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1512A>C
ENST00000471071.2:c.252A>C	ENSP00000493073.2:p.Glu84Asp
ENST00000640756.2:n.317A>C
ENST00000659065.2:c.390A>C	ENSP00000499588.1:p.Glu130Asp
ENST00000659642.2:c.390A>C	ENSP00000499509.1:p.Glu130Asp
ENST00000664374.2:c.390A>C	ENSP00000499664.1:p.Glu130Asp
ENST00000640756.1:n.306A>C
ENST00000659065.1:c.390A>C	ENSP00000499588.1:p.Glu130Asp
ENST00000659642.1:c.390A>C	ENSP00000499509.1:p.Glu130Asp
ENST00000664374.1:c.390A>C	ENSP00000499664.1:p.Glu130Asp
ENST00000423557.1:c.507A>C MANE Select	ENSP00000412237.1:p.Glu169Asp
NM_000572.2:c.507A>C	NP_000563.1:p.Glu169Asp
XM_011509506.1:c.507A>C	XP_011507808.1:p.Glu169Asp
NM_000572.3:c.507A>C MANE Select	NP_000563.1:p.Glu169Asp
NM_001382624.1:c.252A>C	NP_001369553.1:p.Glu84Asp
NR_168466.1:n.804A>C
NR_168467.1:n.334A>C