Canonical Allele Identifier: CA14429431
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs141539546
gnomAD v2: 17-4637378-C-T
gnomAD v3: 17-4734083-C-T
gnomAD v4: 17-4734083-C-T
MyVariant Identifiers: chr17:g.4637378C>T (hg19) chr17:g.4734083C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734083C>T , CM000679.2:g.4734083C>T GRCh38
NC_000017.10:g.4637378C>T , CM000679.1:g.4637378C>T GRCh37
NC_000017.9:g.4584127C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*420G>A MANE Select ENSP00000293778.7:n.*420G>A
ENST00000293778.10:c.*420G>A ENSP00000293778.6:n.*420G>A
ENST00000576153.5:n.976G>A
NM_022059.3:c.*420G>A NP_071342.2:n.*420G>A
NM_022059.4:c.*420G>A NP_071342.2:n.*420G>A
NM_001386809.1:c.*420G>A MANE Select NP_001373738.1:n.*420G>A
Search 100 bp 5'
Search 100 bp 3'