Canonical Allele Identifier: CA287188191
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs555169610
gnomAD v3: 17-4734037-GTC-G
gnomAD v4: 17-4734037-GTC-G
MyVariant Identifiers: chr17:g.4637333_4637334del (hg19) chr17:g.4734038_4734039del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734041_4734042del , CM000679.2:g.4734041_4734042del GRCh38
NC_000017.10:g.4637336_4637337del , CM000679.1:g.4637336_4637337del GRCh37
NC_000017.9:g.4584085_4584086del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*464_*465del MANE Select ENSP00000293778.7:n.*464_*465del
ENST00000293778.10:c.*464_*465del ENSP00000293778.6:n.*464_*465del
ENST00000576153.5:n.1020_1021del
NM_022059.3:c.*464_*465del NP_071342.2:n.*464_*465del
NM_022059.4:c.*464_*465del NP_071342.2:n.*464_*465del
NM_001386809.1:c.*464_*465del MANE Select NP_001373738.1:n.*464_*465del
Search 100 bp 5'
Search 100 bp 3'