Canonical Allele Identifier: CA2483126930

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206771817G= , CM000663.2:g.206771817G= GRCh38
NC_000001.10:g.206945162G= , CM000663.1:g.206945162G= GRCh37
NC_000001.9:g.205011785G= NCBI36
NG_012088.1:g.5678C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000659065.2:c.49-402C= (IL10) ENSP00000499588.1:n.49-402C=
ENST00000659642.2:c.49-402C= (IL10) ENSP00000499509.1:n.49-402C=
ENST00000664374.2:c.49-402C= (IL10) ENSP00000499664.1:n.49-402C=
ENST00000659997.3:c.-149+739G= (IL19) MANE Select ENSP00000499459.2:n.-149+739G=
ENST00000656872.2:c.-149+987G= (IL19) ENSP00000499487.2:n.-149+987G=
ENST00000659065.1:c.49-402C= (IL10) ENSP00000499588.1:n.49-402C=
ENST00000659642.1:c.49-402C= (IL10) ENSP00000499509.1:n.49-402C=
ENST00000659997.2:c.-149+739G= (IL19) ENSP00000499459.2:n.-149+739G=
ENST00000662320.1:n.67+987G= (IL19)
ENST00000664374.1:c.49-402C= (IL10) ENSP00000499664.1:n.49-402C=
ENST00000423557.1:c.166-402C= (IL10) MANE Select ENSP00000412237.1:n.166-402C=
NM_000572.2:c.166-402C= (IL10) NP_000563.1:n.166-402C=
XM_011509506.1:c.166-402C= (IL10) XP_011507808.1:n.166-402C=
NM_000572.3:c.166-402C= (IL10) MANE Select NP_000563.1:n.166-402C=
NM_153758.3:c.-35+739G= (IL19) NP_715639.1:n.-35+739G=
NM_001393490.1:c.-149+987G= (IL19) NP_001380419.1:n.-149+987G=
NM_153758.5:c.-149+739G= (IL19) MANE Select NP_715639.2:n.-149+739G=
NR_168466.1:n.225-402C= (IL10)