Canonical Allele Identifier: CA980962192
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs927878135
gnomAD v3: 17-4734423-G-A
gnomAD v4: 17-4734423-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734423G>A , CM000679.2:g.4734423G>A GRCh38
NC_000017.10:g.4637718G>A , CM000679.1:g.4637718G>A GRCh37
NC_000017.9:g.4584467G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*80C>T MANE Select ENSP00000293778.7:n.*80C>T
ENST00000574412.6:c.*183C>T ENSP00000459592.2:n.*183C>T
ENST00000293778.10:c.*80C>T ENSP00000293778.6:n.*80C>T
ENST00000574412.5:c.*183C>T ENSP00000459592.1:n.*183C>T
ENST00000576153.5:n.636C>T
NM_022059.3:c.*80C>T NP_071342.2:n.*80C>T
NM_022059.4:c.*80C>T NP_071342.2:n.*80C>T
NM_001386809.1:c.*80C>T MANE Select NP_001373738.1:n.*80C>T
Search 100 bp 5'
Search 100 bp 3'