Canonical Allele Identifier: CA980961957
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1362232492
gnomAD v3: 17-4734019-T-C
gnomAD v4: 17-4734019-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734019T>C , CM000679.2:g.4734019T>C GRCh38
NC_000017.10:g.4637314T>C , CM000679.1:g.4637314T>C GRCh37
NC_000017.9:g.4584063T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*484A>G MANE Select ENSP00000293778.7:n.*484A>G
ENST00000293778.10:c.*484A>G ENSP00000293778.6:n.*484A>G
ENST00000576153.5:n.1040A>G
NM_022059.3:c.*484A>G NP_071342.2:n.*484A>G
NM_022059.4:c.*484A>G NP_071342.2:n.*484A>G
NM_001386809.1:c.*484A>G MANE Select NP_001373738.1:n.*484A>G
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