Canonical Allele Identifier: CA2483127494

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206773094C= , CM000663.2:g.206773094C= GRCh38
NC_000001.10:g.206946439C= , CM000663.1:g.206946439C= GRCh37
NC_000001.9:g.205013062C= NCBI36
NG_012088.1:g.4401G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000659065.2:c.-15+586G= (IL10) ENSP00000499588.1:n.-15+586G=
ENST00000659642.2:c.-776G= (IL10) ENSP00000499509.1:n.-776G=
ENST00000664374.2:c.-14-762G= (IL10) ENSP00000499664.1:n.-14-762G=
ENST00000659997.3:c.-149+2016C= (IL19) MANE Select ENSP00000499459.2:n.-149+2016C=
ENST00000656872.2:c.-149+2264C= (IL19) ENSP00000499487.2:n.-149+2264C=
ENST00000659065.1:c.-15+586G= (IL10) ENSP00000499588.1:n.-15+586G=
ENST00000659642.1:c.-776G= (IL10) ENSP00000499509.1:n.-776G=
ENST00000659997.2:c.-149+2016C= (IL19) ENSP00000499459.2:n.-149+2016C=
ENST00000662320.1:n.67+2264C= (IL19)
ENST00000664374.1:c.-14-762G= (IL10) ENSP00000499664.1:n.-14-762G=
XM_011509506.1:c.-659G= (IL10) XP_011507808.1:n.-659G=
NM_153758.3:c.-35+2016C= (IL19) NP_715639.1:n.-35+2016C=
NM_001393490.1:c.-149+2264C= (IL19) NP_001380419.1:n.-149+2264C=
NM_153758.5:c.-149+2016C= (IL19) MANE Select NP_715639.2:n.-149+2016C=