Canonical Allele Identifier: CA2635549901
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734174-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734174C>A , CM000679.2:g.4734174C>A GRCh38
NC_000017.10:g.4637469C>A , CM000679.1:g.4637469C>A GRCh37
NC_000017.9:g.4584218C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*329G>T MANE Select ENSP00000293778.7:n.*329G>T
ENST00000293778.10:c.*329G>T ENSP00000293778.6:n.*329G>T
ENST00000576153.5:n.885G>T
NM_022059.3:c.*329G>T NP_071342.2:n.*329G>T
NM_022059.4:c.*329G>T NP_071342.2:n.*329G>T
NM_001386809.1:c.*329G>T MANE Select NP_001373738.1:n.*329G>T
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