Canonical Allele Identifier: CA624612217
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1555563004
gnomAD v2: 17-4637331-C-CA
gnomAD v3: 17-4734036-C-CA
gnomAD v4: 17-4734036-C-CA
MyVariant Identifiers: chr17:g.4637331_4637332insA (hg19) chr17:g.4734036_4734037insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734036_4734037insA , CM000679.2:g.4734036_4734037insA GRCh38
NC_000017.10:g.4637331_4637332insA , CM000679.1:g.4637331_4637332insA GRCh37
NC_000017.9:g.4584080_4584081insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*466_*467insT MANE Select ENSP00000293778.7:n.*466_*467insT
ENST00000293778.10:c.*466_*467insT ENSP00000293778.6:n.*466_*467insT
ENST00000576153.5:n.1022_1023insT
NM_022059.3:c.*466_*467insT NP_071342.2:n.*466_*467insT
NM_022059.4:c.*466_*467insT NP_071342.2:n.*466_*467insT
NM_001386809.1:c.*466_*467insT MANE Select NP_001373738.1:n.*466_*467insT
Search 100 bp 5'
Search 100 bp 3'