Canonical Allele Identifier: CA344482194

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206771031T>C , CM000663.2:g.206771031T>C GRCh38
NC_000001.10:g.206944376T>C , CM000663.1:g.206944376T>C GRCh37
NC_000001.9:g.205010999T>C NCBI36
NG_012088.1:g.6464A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367099.4:n.159A>G (IL10)
ENST00000471071.2:c.-2A>G (IL10) ENSP00000493073.2:n.-2A>G
ENST00000659065.2:c.137A>G (IL10) ENSP00000499588.1:p.Glu46Gly
ENST00000659642.2:c.137A>G (IL10) ENSP00000499509.1:p.Glu46Gly
ENST00000664374.2:c.137A>G (IL10) ENSP00000499664.1:p.Glu46Gly
ENST00000659997.3:c.-196T>C (IL19) MANE Select ENSP00000499459.2:n.-196T>C
ENST00000656872.2:c.-149+201T>C (IL19) ENSP00000499487.2:n.-149+201T>C
ENST00000659065.1:c.137A>G (IL10) ENSP00000499588.1:p.Glu46Gly
ENST00000659642.1:c.137A>G (IL10) ENSP00000499509.1:p.Glu46Gly
ENST00000659997.2:c.-196T>C (IL19) ENSP00000499459.2:n.-196T>C
ENST00000662320.1:n.67+201T>C (IL19)
ENST00000664374.1:c.137A>G (IL10) ENSP00000499664.1:p.Glu46Gly
ENST00000367099.3:n.159A>G (IL10)
ENST00000423557.1:c.254A>G (IL10) MANE Select ENSP00000412237.1:p.Glu85Gly
ENST00000471071.1:n.169A>G (IL10)
NM_000572.2:c.254A>G (IL10) NP_000563.1:p.Glu85Gly
XM_011509506.1:c.254A>G (IL10) XP_011507808.1:p.Glu85Gly
NM_000572.3:c.254A>G (IL10) MANE Select NP_000563.1:p.Glu85Gly
NM_153758.3:c.-82T>C (IL19) NP_715639.1:n.-82T>C
NM_001382624.1:c.-2A>G (IL10) NP_001369553.1:n.-2A>G
NM_001393490.1:c.-149+201T>C (IL19) NP_001380419.1:n.-149+201T>C
NM_153758.5:c.-196T>C (IL19) MANE Select NP_715639.2:n.-196T>C
NR_168466.1:n.313A>G (IL10)