Canonical Allele Identifier: CA2808290849
Gene: CXCL16 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734087T>A , CM000679.2:g.4734087T>A GRCh38
NC_000017.10:g.4637382T>A , CM000679.1:g.4637382T>A GRCh37
NC_000017.9:g.4584131T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*416A>T MANE Select ENSP00000293778.7:n.*416A>T
ENST00000293778.10:c.*416A>T ENSP00000293778.6:n.*416A>T
ENST00000576153.5:n.972A>T
NM_022059.3:c.*416A>T NP_071342.2:n.*416A>T
NM_022059.4:c.*416A>T NP_071342.2:n.*416A>T
NM_001386809.1:c.*416A>T MANE Select NP_001373738.1:n.*416A>T
Search 100 bp 5'
Search 100 bp 3'