Canonical Allele Identifier: CA2483128755
Gene: IL19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206776063G= , CM000663.2:g.206776063G= GRCh38
NC_000001.10:g.206949408G= , CM000663.1:g.206949408G= GRCh37
NC_000001.9:g.205016031G= NCBI36
NG_012088.1:g.1432C=

Transcript Alleles

HGVS Amino-acid change
ENST00000659997.3:c.-149+4985G= MANE Select ENSP00000499459.2:n.-149+4985G=
ENST00000656872.2:c.-149+5233G= ENSP00000499487.2:n.-149+5233G=
ENST00000659997.2:c.-149+4985G= ENSP00000499459.2:n.-149+4985G=
ENST00000662320.1:n.67+5233G=
NM_153758.3:c.-35+4985G= NP_715639.1:n.-35+4985G=
NM_001393490.1:c.-149+5233G= NP_001380419.1:n.-149+5233G=
NM_153758.5:c.-149+4985G= MANE Select NP_715639.2:n.-149+4985G=