Canonical Allele Identifier: CA2244533364
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734113G= , CM000679.2:g.4734113G= GRCh38
NC_000017.10:g.4637408G= , CM000679.1:g.4637408G= GRCh37
NC_000017.9:g.4584157G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*390C= MANE Select ENSP00000293778.7:n.*390C=
ENST00000293778.10:c.*390C= ENSP00000293778.6:n.*390C=
ENST00000576153.5:n.946C=
NM_022059.3:c.*390C= NP_071342.2:n.*390C=
NM_022059.4:c.*390C= NP_071342.2:n.*390C=
NM_001386809.1:c.*390C= MANE Select NP_001373738.1:n.*390C=