Canonical Allele Identifier: CA287188469
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs749663954
gnomAD v3: 17-4734490-A-G
gnomAD v4: 17-4734490-A-G
MyVariant Identifiers: chr17:g.4637785A>G (hg19) chr17:g.4734490A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734490A>G , CM000679.2:g.4734490A>G GRCh38
NC_000017.10:g.4637785A>G , CM000679.1:g.4637785A>G GRCh37
NC_000017.9:g.4584534A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*24-11T>C MANE Select ENSP00000293778.7:n.*24-11T>C
ENST00000574412.6:c.*116T>C ENSP00000459592.2:n.*116T>C
ENST00000293778.10:c.*24-11T>C ENSP00000293778.6:n.*24-11T>C
ENST00000574412.5:c.*116T>C ENSP00000459592.1:n.*116T>C
ENST00000576153.5:n.580-11T>C
NM_022059.3:c.*24-11T>C NP_071342.2:n.*24-11T>C
NM_022059.4:c.*24-11T>C NP_071342.2:n.*24-11T>C
NM_001386809.1:c.*24-11T>C MANE Select NP_001373738.1:n.*24-11T>C
Search 100 bp 5'
Search 100 bp 3'