Canonical Allele Identifier: CA2580574918
Gene: IL10 HGNC NCBI
IL19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206773062T>A , CM000663.2:g.206773062T>A GRCh38
NC_000001.10:g.206946407T>A , CM000663.1:g.206946407T>A GRCh37
NC_000001.9:g.205013030T>A NCBI36
NG_012088.1:g.4433A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000659065.2:c.-15+618A>T (IL10) ENSP00000499588.1:n.-15+618A>T
ENST00000659642.2:c.-744A>T (IL10) ENSP00000499509.1:n.-744A>T
ENST00000664374.2:c.-14-730A>T (IL10) ENSP00000499664.1:n.-14-730A>T
ENST00000659997.3:c.-149+1984T>A (IL19) MANE Select ENSP00000499459.2:n.-149+1984T>A
ENST00000656872.2:c.-149+2232T>A (IL19) ENSP00000499487.2:n.-149+2232T>A
ENST00000659065.1:c.-15+618A>T (IL10) ENSP00000499588.1:n.-15+618A>T
ENST00000659642.1:c.-744A>T (IL10) ENSP00000499509.1:n.-744A>T
ENST00000659997.2:c.-149+1984T>A (IL19) ENSP00000499459.2:n.-149+1984T>A
ENST00000662320.1:n.67+2232T>A (IL19)
ENST00000664374.1:c.-14-730A>T (IL10) ENSP00000499664.1:n.-14-730A>T
XM_011509506.1:c.-627A>T (IL10) XP_011507808.1:n.-627A>T
NM_153758.3:c.-35+1984T>A (IL19) NP_715639.1:n.-35+1984T>A
NM_001393490.1:c.-149+2232T>A (IL19) NP_001380419.1:n.-149+2232T>A
NM_153758.5:c.-149+1984T>A (IL19) MANE Select NP_715639.2:n.-149+1984T>A
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