Canonical Allele Identifier: CA287188451
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1051473561
gnomAD v2: 17-4637771-G-A
gnomAD v3: 17-4734476-G-A
gnomAD v4: 17-4734476-G-A
MyVariant Identifiers: chr17:g.4637771G>A (hg19) chr17:g.4734476G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734476G>A , CM000679.2:g.4734476G>A GRCh38
NC_000017.10:g.4637771G>A , CM000679.1:g.4637771G>A GRCh37
NC_000017.9:g.4584520G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*27C>T MANE Select ENSP00000293778.7:n.*27C>T
ENST00000574412.6:c.*130C>T ENSP00000459592.2:n.*130C>T
ENST00000293778.10:c.*27C>T ENSP00000293778.6:n.*27C>T
ENST00000574412.5:c.*130C>T ENSP00000459592.1:n.*130C>T
ENST00000576153.5:n.583C>T
NM_022059.3:c.*27C>T NP_071342.2:n.*27C>T
NM_022059.4:c.*27C>T NP_071342.2:n.*27C>T
NM_001386809.1:c.*27C>T MANE Select NP_001373738.1:n.*27C>T
Search 100 bp 5'
Search 100 bp 3'