Canonical Allele Identifier: CA2190785519
Gene: IL16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.81185015T= , CM000677.2:g.81185015T= GRCh38
NC_000015.9:g.81477356T= , CM000677.1:g.81477356T= GRCh37
NC_000015.8:g.79264411T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000302987.10:c.40+2119T= ENSP00000302935.5:n.40+2119T=
ENST00000302987.9:c.40+2119T= ENSP00000302935.5:n.40+2119T=
ENST00000360547.9:c.-153+2119T= ENSP00000456972.1:n.-153+2119T=
ENST00000560241.5:c.-102+2119T= ENSP00000452738.1:n.-102+2119T=
XM_005254342.2:c.40+2119T= XP_005254399.1:n.40+2119T=
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