Canonical Allele Identifier: CA2244533348
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734100T= , CM000679.2:g.4734100T= GRCh38
NC_000017.10:g.4637395T= , CM000679.1:g.4637395T= GRCh37
NC_000017.9:g.4584144T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*403A= MANE Select ENSP00000293778.7:n.*403A=
ENST00000293778.10:c.*403A= ENSP00000293778.6:n.*403A=
ENST00000576153.5:n.959A=
NM_022059.3:c.*403A= NP_071342.2:n.*403A=
NM_022059.4:c.*403A= NP_071342.2:n.*403A=
NM_001386809.1:c.*403A= MANE Select NP_001373738.1:n.*403A=