Canonical Allele Identifier: CA2244533232
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734025T= , CM000679.2:g.4734025T= GRCh38
NC_000017.10:g.4637320T= , CM000679.1:g.4637320T= GRCh37
NC_000017.9:g.4584069T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*478A= MANE Select ENSP00000293778.7:n.*478A=
ENST00000293778.10:c.*478A= ENSP00000293778.6:n.*478A=
ENST00000576153.5:n.1034A=
NM_022059.3:c.*478A= NP_071342.2:n.*478A=
NM_022059.4:c.*478A= NP_071342.2:n.*478A=
NM_001386809.1:c.*478A= MANE Select NP_001373738.1:n.*478A=