Canonical Allele Identifier: CA2483128774
Gene: IL19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206776106T= , CM000663.2:g.206776106T= GRCh38
NC_000001.10:g.206949451T= , CM000663.1:g.206949451T= GRCh37
NC_000001.9:g.205016074T= NCBI36
NG_012088.1:g.1389A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000659997.3:c.-149+5028T= MANE Select ENSP00000499459.2:n.-149+5028T=
ENST00000656872.2:c.-149+5276T= ENSP00000499487.2:n.-149+5276T=
ENST00000659997.2:c.-149+5028T= ENSP00000499459.2:n.-149+5028T=
ENST00000662320.1:n.67+5276T=
NM_153758.3:c.-35+5028T= NP_715639.1:n.-35+5028T=
NM_001393490.1:c.-149+5276T= NP_001380419.1:n.-149+5276T=
NM_153758.5:c.-149+5028T= MANE Select NP_715639.2:n.-149+5028T=
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