Canonical Allele Identifier: CA2483127431

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206772966T= , CM000663.2:g.206772966T= GRCh38
NC_000001.10:g.206946311T= , CM000663.1:g.206946311T= GRCh37
NC_000001.9:g.205012934T= NCBI36
NG_012088.1:g.4529A=

Transcript Alleles

HGVS Amino-acid change
ENST00000659065.2:c.-14-634A= (IL10) ENSP00000499588.1:n.-14-634A=
ENST00000659642.2:c.-648A= (IL10) ENSP00000499509.1:n.-648A=
ENST00000664374.2:c.-14-634A= (IL10) ENSP00000499664.1:n.-14-634A=
ENST00000659997.3:c.-149+1888T= (IL19) MANE Select ENSP00000499459.2:n.-149+1888T=
ENST00000656872.2:c.-149+2136T= (IL19) ENSP00000499487.2:n.-149+2136T=
ENST00000659065.1:c.-14-634A= (IL10) ENSP00000499588.1:n.-14-634A=
ENST00000659642.1:c.-648A= (IL10) ENSP00000499509.1:n.-648A=
ENST00000659997.2:c.-149+1888T= (IL19) ENSP00000499459.2:n.-149+1888T=
ENST00000662320.1:n.67+2136T= (IL19)
ENST00000664374.1:c.-14-634A= (IL10) ENSP00000499664.1:n.-14-634A=
XM_011509506.1:c.-531A= (IL10) XP_011507808.1:n.-531A=
NM_153758.3:c.-35+1888T= (IL19) NP_715639.1:n.-35+1888T=
NM_001393490.1:c.-149+2136T= (IL19) NP_001380419.1:n.-149+2136T=
NM_153758.5:c.-149+1888T= (IL19) MANE Select NP_715639.2:n.-149+1888T=