Canonical Allele Identifier: CA980961962
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1916075302

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734036del , CM000679.2:g.4734036del GRCh38
NC_000017.10:g.4637331del , CM000679.1:g.4637331del GRCh37
NC_000017.9:g.4584080del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*470del MANE Select ENSP00000293778.7:n.*470del
ENST00000293778.10:c.*470del ENSP00000293778.6:n.*470del
ENST00000576153.5:n.1026del
NM_022059.3:c.*470del NP_071342.2:n.*470del
NM_022059.4:c.*470del NP_071342.2:n.*470del
NM_001386809.1:c.*470del MANE Select NP_001373738.1:n.*470del