Canonical Allele Identifier: CA2808290867
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734230C>G , CM000679.2:g.4734230C>G GRCh38
NC_000017.10:g.4637525C>G , CM000679.1:g.4637525C>G GRCh37
NC_000017.9:g.4584274C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*273G>C MANE Select ENSP00000293778.7:n.*273G>C
ENST00000293778.10:c.*273G>C ENSP00000293778.6:n.*273G>C
ENST00000576153.5:n.829G>C
NM_022059.3:c.*273G>C NP_071342.2:n.*273G>C
NM_022059.4:c.*273G>C NP_071342.2:n.*273G>C
NM_001386809.1:c.*273G>C MANE Select NP_001373738.1:n.*273G>C