Canonical Allele Identifier: CA16077425
Gene: IL10 HGNC NCBI

Linked Data

dbSNP Id: rs3024509
gnomAD v2: 1-206943297-A-G
gnomAD v3: 1-206769952-A-G
gnomAD v4: 1-206769952-A-G
MyVariant Identifiers: chr1:g.206943297A>G (hg19) chr1:g.206769952A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206769952A>G , CM000663.2:g.206769952A>G GRCh38
NC_000001.10:g.206943297A>G , CM000663.1:g.206943297A>G GRCh37
NC_000001.9:g.205009920A>G NCBI36
NG_012088.1:g.7543T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367099.4:n.284-58T>C
ENST00000471071.2:c.124-58T>C ENSP00000493073.2:n.124-58T>C
ENST00000640756.2:n.189-58T>C
ENST00000659065.2:c.262-58T>C ENSP00000499588.1:n.262-58T>C
ENST00000659642.2:c.262-58T>C ENSP00000499509.1:n.262-58T>C
ENST00000664374.2:c.262-58T>C ENSP00000499664.1:n.262-58T>C
ENST00000640756.1:n.178-58T>C
ENST00000659065.1:c.262-58T>C ENSP00000499588.1:n.262-58T>C
ENST00000659642.1:c.262-58T>C ENSP00000499509.1:n.262-58T>C
ENST00000664374.1:c.262-58T>C ENSP00000499664.1:n.262-58T>C
ENST00000367099.3:n.284-58T>C
ENST00000423557.1:c.379-58T>C MANE Select ENSP00000412237.1:n.379-58T>C
ENST00000471071.1:n.294-58T>C
NM_000572.2:c.379-58T>C NP_000563.1:n.379-58T>C
XM_011509506.1:c.379-58T>C XP_011507808.1:n.379-58T>C
NM_000572.3:c.379-58T>C MANE Select NP_000563.1:n.379-58T>C
NM_001382624.1:c.124-58T>C NP_001369553.1:n.124-58T>C
NR_168466.1:n.676-58T>C
NR_168467.1:n.206-58T>C
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