Canonical Allele Identifier: CA772506802
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1162574571
gnomAD v3: 17-4734053-C-CA
gnomAD v4: 17-4734053-C-CA
MyVariant Identifiers: chr17:g.4637348_4637349insA (hg19) chr17:g.4734053_4734054insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734059dup , CM000679.2:g.4734059dup GRCh38
NC_000017.10:g.4637354dup , CM000679.1:g.4637354dup GRCh37
NC_000017.9:g.4584103dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*449dup MANE Select ENSP00000293778.7:n.*449dup
ENST00000293778.10:c.*449dup ENSP00000293778.6:n.*449dup
ENST00000576153.5:n.1005dup
NM_022059.3:c.*449dup NP_071342.2:n.*449dup
NM_022059.4:c.*449dup NP_071342.2:n.*449dup
NM_001386809.1:c.*449dup MANE Select NP_001373738.1:n.*449dup
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