Canonical Allele Identifier: CA287188286
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs898871045
gnomAD v3: 17-4734125-GA-G
gnomAD v4: 17-4734125-GA-G
MyVariant Identifiers: chr17:g.4637421del (hg19) chr17:g.4734126del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734127del , CM000679.2:g.4734127del GRCh38
NC_000017.10:g.4637422del , CM000679.1:g.4637422del GRCh37
NC_000017.9:g.4584171del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*377del MANE Select ENSP00000293778.7:n.*377del
ENST00000293778.10:c.*377del ENSP00000293778.6:n.*377del
ENST00000576153.5:n.933del
NM_022059.3:c.*377del NP_071342.2:n.*377del
NM_022059.4:c.*377del NP_071342.2:n.*377del
NM_001386809.1:c.*377del MANE Select NP_001373738.1:n.*377del
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