Canonical Allele Identifier: CA287188340
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs765107028
gnomAD v3: 17-4734222-AAAC-A
gnomAD v4: 17-4734222-AAAC-A
MyVariant Identifiers: chr17:g.4637518_4637520del (hg19) chr17:g.4734223_4734225del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734225_4734227del , CM000679.2:g.4734225_4734227del GRCh38
NC_000017.10:g.4637520_4637522del , CM000679.1:g.4637520_4637522del GRCh37
NC_000017.9:g.4584269_4584271del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*278_*280del MANE Select ENSP00000293778.7:n.*278_*280del
ENST00000293778.10:c.*278_*280del ENSP00000293778.6:n.*278_*280del
ENST00000576153.5:n.834_836del
NM_022059.3:c.*278_*280del NP_071342.2:n.*278_*280del
NM_022059.4:c.*278_*280del NP_071342.2:n.*278_*280del
NM_001386809.1:c.*278_*280del MANE Select NP_001373738.1:n.*278_*280del
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