Canonical Allele Identifier: CA2244533278
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734055A= , CM000679.2:g.4734055A= GRCh38
NC_000017.10:g.4637350A= , CM000679.1:g.4637350A= GRCh37
NC_000017.9:g.4584099A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*448T= MANE Select ENSP00000293778.7:n.*448T=
ENST00000293778.10:c.*448T= ENSP00000293778.6:n.*448T=
ENST00000576153.5:n.1004T=
NM_022059.3:c.*448T= NP_071342.2:n.*448T=
NM_022059.4:c.*448T= NP_071342.2:n.*448T=
NM_001386809.1:c.*448T= MANE Select NP_001373738.1:n.*448T=