Canonical Allele Identifier: CA287188296
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1050058864
gnomAD v3: 17-4734133-G-A
gnomAD v4: 17-4734133-G-A
MyVariant Identifiers: chr17:g.4637428G>A (hg19) chr17:g.4734133G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734133G>A , CM000679.2:g.4734133G>A GRCh38
NC_000017.10:g.4637428G>A , CM000679.1:g.4637428G>A GRCh37
NC_000017.9:g.4584177G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*370C>T MANE Select ENSP00000293778.7:n.*370C>T
ENST00000293778.10:c.*370C>T ENSP00000293778.6:n.*370C>T
ENST00000576153.5:n.926C>T
NM_022059.3:c.*370C>T NP_071342.2:n.*370C>T
NM_022059.4:c.*370C>T NP_071342.2:n.*370C>T
NM_001386809.1:c.*370C>T MANE Select NP_001373738.1:n.*370C>T
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