Canonical Allele Identifier: CA980962404
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1916094296
gnomAD v3: 17-4734569-A-T
gnomAD v4: 17-4734569-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734569A>T , CM000679.2:g.4734569A>T GRCh38
NC_000017.10:g.4637864A>T , CM000679.1:g.4637864A>T GRCh37
NC_000017.9:g.4584613A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*23+14T>A MANE Select ENSP00000293778.7:n.*23+14T>A
ENST00000574412.6:c.*37T>A ENSP00000459592.2:n.*37T>A
ENST00000293778.10:c.*23+14T>A ENSP00000293778.6:n.*23+14T>A
ENST00000574412.5:c.*37T>A ENSP00000459592.1:n.*37T>A
ENST00000576153.5:n.579+14T>A
NM_001100812.1:c.*37T>A NP_001094282.1:n.*37T>A
NM_022059.3:c.*23+14T>A NP_071342.2:n.*23+14T>A
NM_022059.4:c.*23+14T>A NP_071342.2:n.*23+14T>A
NM_001100812.2:c.*37T>A NP_001094282.2:n.*37T>A
NM_001386809.1:c.*23+14T>A MANE Select NP_001373738.1:n.*23+14T>A
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