Canonical Allele Identifier: CA772506771
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1362232492
gnomAD v4: 17-4734019-T-A
MyVariant Identifiers: chr17:g.4637314T>A (hg19) chr17:g.4734019T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734019T>A , CM000679.2:g.4734019T>A GRCh38
NC_000017.10:g.4637314T>A , CM000679.1:g.4637314T>A GRCh37
NC_000017.9:g.4584063T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*484A>T MANE Select ENSP00000293778.7:n.*484A>T
ENST00000293778.10:c.*484A>T ENSP00000293778.6:n.*484A>T
ENST00000576153.5:n.1040A>T
NM_022059.3:c.*484A>T NP_071342.2:n.*484A>T
NM_022059.4:c.*484A>T NP_071342.2:n.*484A>T
NM_001386809.1:c.*484A>T MANE Select NP_001373738.1:n.*484A>T
Search 100 bp 5'
Search 100 bp 3'