Canonical Allele Identifier: CA980962004
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v3: 17-4734069-T-C
gnomAD v4: 17-4734069-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734069T>C , CM000679.2:g.4734069T>C GRCh38
NC_000017.10:g.4637364T>C , CM000679.1:g.4637364T>C GRCh37
NC_000017.9:g.4584113T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*434A>G MANE Select ENSP00000293778.7:n.*434A>G
ENST00000293778.10:c.*434A>G ENSP00000293778.6:n.*434A>G
ENST00000576153.5:n.990A>G
NM_022059.3:c.*434A>G NP_071342.2:n.*434A>G
NM_022059.4:c.*434A>G NP_071342.2:n.*434A>G
NM_001386809.1:c.*434A>G MANE Select NP_001373738.1:n.*434A>G
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