Canonical Allele Identifier: CA2808290879
Gene: CXCL16 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734318A>G , CM000679.2:g.4734318A>G GRCh38
NC_000017.10:g.4637613A>G , CM000679.1:g.4637613A>G GRCh37
NC_000017.9:g.4584362A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*185T>C MANE Select ENSP00000293778.7:n.*185T>C
ENST00000574412.6:c.*288T>C ENSP00000459592.2:n.*288T>C
ENST00000293778.10:c.*185T>C ENSP00000293778.6:n.*185T>C
ENST00000574412.5:c.*288T>C ENSP00000459592.1:n.*288T>C
ENST00000576153.5:n.741T>C
NM_022059.3:c.*185T>C NP_071342.2:n.*185T>C
NM_022059.4:c.*185T>C NP_071342.2:n.*185T>C
NM_001386809.1:c.*185T>C MANE Select NP_001373738.1:n.*185T>C
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