Canonical Allele Identifier: CA2635549764
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734113-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734113G>C , CM000679.2:g.4734113G>C GRCh38
NC_000017.10:g.4637408G>C , CM000679.1:g.4637408G>C GRCh37
NC_000017.9:g.4584157G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*390C>G MANE Select ENSP00000293778.7:n.*390C>G
ENST00000293778.10:c.*390C>G ENSP00000293778.6:n.*390C>G
ENST00000576153.5:n.946C>G
NM_022059.3:c.*390C>G NP_071342.2:n.*390C>G
NM_022059.4:c.*390C>G NP_071342.2:n.*390C>G
NM_001386809.1:c.*390C>G MANE Select NP_001373738.1:n.*390C>G
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