Canonical Allele Identifier: CA2483128733
Gene: IL19 HGNC NCBI

Linked Data

dbSNP Id: rs1674981466
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206776019_206776020insT , CM000663.2:g.206776019_206776020insT GRCh38
NC_000001.10:g.206949364_206949365insT , CM000663.1:g.206949364_206949365insT GRCh37
NC_000001.9:g.205015987_205015988insT NCBI36
NG_012088.1:g.1475_1476insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000659997.3:c.-149+4941_-149+4942insT MANE Select ENSP00000499459.2:n.-149+4941_-149+4942insT
ENST00000656872.2:c.-149+5189_-149+5190insT ENSP00000499487.2:n.-149+5189_-149+5190insT
ENST00000659997.2:c.-149+4941_-149+4942insT ENSP00000499459.2:n.-149+4941_-149+4942insT
ENST00000662320.1:n.67+5189_67+5190insT
NM_153758.3:c.-35+4941_-35+4942insT NP_715639.1:n.-35+4941_-35+4942insT
NM_001393490.1:c.-149+5189_-149+5190insT NP_001380419.1:n.-149+5189_-149+5190insT
NM_153758.5:c.-149+4941_-149+4942insT MANE Select NP_715639.2:n.-149+4941_-149+4942insT
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