Canonical Allele Identifier: CA980961958
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v3: 17-4734025-T-G
gnomAD v4: 17-4734025-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734025T>G , CM000679.2:g.4734025T>G GRCh38
NC_000017.10:g.4637320T>G , CM000679.1:g.4637320T>G GRCh37
NC_000017.9:g.4584069T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*478A>C MANE Select ENSP00000293778.7:n.*478A>C
ENST00000293778.10:c.*478A>C ENSP00000293778.6:n.*478A>C
ENST00000576153.5:n.1034A>C
NM_022059.3:c.*478A>C NP_071342.2:n.*478A>C
NM_022059.4:c.*478A>C NP_071342.2:n.*478A>C
NM_001386809.1:c.*478A>C MANE Select NP_001373738.1:n.*478A>C
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