Canonical Allele Identifier: CA624612220
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1340965176
gnomAD v2: 17-4637355-T-C
gnomAD v3: 17-4734060-T-C
gnomAD v4: 17-4734060-T-C
MyVariant Identifiers: chr17:g.4637355T>C (hg19) chr17:g.4734060T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734060T>C , CM000679.2:g.4734060T>C GRCh38
NC_000017.10:g.4637355T>C , CM000679.1:g.4637355T>C GRCh37
NC_000017.9:g.4584104T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*443A>G MANE Select ENSP00000293778.7:n.*443A>G
ENST00000293778.10:c.*443A>G ENSP00000293778.6:n.*443A>G
ENST00000576153.5:n.999A>G
NM_022059.3:c.*443A>G NP_071342.2:n.*443A>G
NM_022059.4:c.*443A>G NP_071342.2:n.*443A>G
NM_001386809.1:c.*443A>G MANE Select NP_001373738.1:n.*443A>G
Search 100 bp 5'
Search 100 bp 3'