Canonical Allele Identifier: CA2635550136
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734431-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734431C>A , CM000679.2:g.4734431C>A GRCh38
NC_000017.10:g.4637726C>A , CM000679.1:g.4637726C>A GRCh37
NC_000017.9:g.4584475C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*72G>T MANE Select ENSP00000293778.7:n.*72G>T
ENST00000574412.6:c.*175G>T ENSP00000459592.2:n.*175G>T
ENST00000293778.10:c.*72G>T ENSP00000293778.6:n.*72G>T
ENST00000574412.5:c.*175G>T ENSP00000459592.1:n.*175G>T
ENST00000576153.5:n.628G>T
NM_022059.3:c.*72G>T NP_071342.2:n.*72G>T
NM_022059.4:c.*72G>T NP_071342.2:n.*72G>T
NM_001386809.1:c.*72G>T MANE Select NP_001373738.1:n.*72G>T