Canonical Allele Identifier: CA2650218366
Gene: IL10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206770708T>C , CM000663.2:g.206770708T>C GRCh38
NC_000001.10:g.206944053T>C , CM000663.1:g.206944053T>C GRCh37
NC_000001.9:g.205010676T>C NCBI36
NG_012088.1:g.6787A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367099.4:n.283+199A>G
ENST00000471071.2:c.123+199A>G ENSP00000493073.2:n.123+199A>G
ENST00000659065.2:c.261+199A>G ENSP00000499588.1:n.261+199A>G
ENST00000659642.2:c.261+199A>G ENSP00000499509.1:n.261+199A>G
ENST00000664374.2:c.261+199A>G ENSP00000499664.1:n.261+199A>G
ENST00000659065.1:c.261+199A>G ENSP00000499588.1:n.261+199A>G
ENST00000659642.1:c.261+199A>G ENSP00000499509.1:n.261+199A>G
ENST00000664374.1:c.261+199A>G ENSP00000499664.1:n.261+199A>G
ENST00000367099.3:n.283+199A>G
ENST00000423557.1:c.378+199A>G MANE Select ENSP00000412237.1:n.378+199A>G
ENST00000471071.1:n.293+199A>G
NM_000572.2:c.378+199A>G NP_000563.1:n.378+199A>G
XM_011509506.1:c.378+199A>G XP_011507808.1:n.378+199A>G
NM_000572.3:c.378+199A>G MANE Select NP_000563.1:n.378+199A>G
NM_001382624.1:c.123+199A>G NP_001369553.1:n.123+199A>G
NR_168466.1:n.437+199A>G