Canonical Allele Identifier: CA2483128722
Gene: IL19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206775991A= , CM000663.2:g.206775991A= GRCh38
NC_000001.10:g.206949336A= , CM000663.1:g.206949336A= GRCh37
NC_000001.9:g.205015959A= NCBI36
NG_012088.1:g.1504T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000659997.3:c.-149+4913A= MANE Select ENSP00000499459.2:n.-149+4913A=
ENST00000656872.2:c.-149+5161A= ENSP00000499487.2:n.-149+5161A=
ENST00000659997.2:c.-149+4913A= ENSP00000499459.2:n.-149+4913A=
ENST00000662320.1:n.67+5161A=
NM_153758.3:c.-35+4913A= NP_715639.1:n.-35+4913A=
NM_001393490.1:c.-149+5161A= NP_001380419.1:n.-149+5161A=
NM_153758.5:c.-149+4913A= MANE Select NP_715639.2:n.-149+4913A=
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