Canonical Allele Identifier: CA980962176
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1916087942
gnomAD v3: 17-4734401-T-C
gnomAD v4: 17-4734401-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734401T>C , CM000679.2:g.4734401T>C GRCh38
NC_000017.10:g.4637696T>C , CM000679.1:g.4637696T>C GRCh37
NC_000017.9:g.4584445T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*102A>G MANE Select ENSP00000293778.7:n.*102A>G
ENST00000574412.6:c.*205A>G ENSP00000459592.2:n.*205A>G
ENST00000293778.10:c.*102A>G ENSP00000293778.6:n.*102A>G
ENST00000574412.5:c.*205A>G ENSP00000459592.1:n.*205A>G
ENST00000576153.5:n.658A>G
NM_022059.3:c.*102A>G NP_071342.2:n.*102A>G
NM_022059.4:c.*102A>G NP_071342.2:n.*102A>G
NM_001386809.1:c.*102A>G MANE Select NP_001373738.1:n.*102A>G
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