Canonical Allele Identifier: CA1363726

Gene: IL10

Linked Data

• ClinVar Variation Id: 662170
• ClinVar RCV Id: RCV000819760
• dbSNP Id: rs768418064
• ExAC: 1:206942004 T / C
• gnomAD v2: 1-206942004-T-C
• gnomAD v3: 1-206768659-T-C
• gnomAD v4: 1-206768659-T-C
• MyVariant Identifiers: chr1:g.206942004T>C (hg19) ; chr1:g.206768659T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.206768659T>C , CM000663.2:g.206768659T>C	GRCh38
NC_000001.10:g.206942004T>C , CM000663.1:g.206942004T>C	GRCh37
NC_000001.9:g.205008627T>C	NCBI36
NG_012088.1:g.8836A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367099.4:n.1519A>G
ENST00000471071.2:c.259A>G	ENSP00000493073.2:p.Met87Val
ENST00000640756.2:n.324A>G
ENST00000659065.2:c.397A>G	ENSP00000499588.1:p.Met133Val
ENST00000659642.2:c.397A>G	ENSP00000499509.1:p.Met133Val
ENST00000664374.2:c.397A>G	ENSP00000499664.1:p.Met133Val
ENST00000640756.1:n.313A>G
ENST00000659065.1:c.397A>G	ENSP00000499588.1:p.Met133Val
ENST00000659642.1:c.397A>G	ENSP00000499509.1:p.Met133Val
ENST00000664374.1:c.397A>G	ENSP00000499664.1:p.Met133Val
ENST00000423557.1:c.514A>G MANE Select	ENSP00000412237.1:p.Met172Val
NM_000572.2:c.514A>G	NP_000563.1:p.Met172Val
XM_011509506.1:c.514A>G	XP_011507808.1:p.Met172Val
NM_000572.3:c.514A>G MANE Select	NP_000563.1:p.Met172Val
NM_001382624.1:c.259A>G	NP_001369553.1:p.Met87Val
NR_168466.1:n.811A>G
NR_168467.1:n.341A>G