Canonical Allele Identifier: CA2635550222
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734501-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734501C>A , CM000679.2:g.4734501C>A GRCh38
NC_000017.10:g.4637796C>A , CM000679.1:g.4637796C>A GRCh37
NC_000017.9:g.4584545C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293778.12:c.*24-22G>T MANE Select ENSP00000293778.7:n.*24-22G>T
ENST00000574412.6:c.*105G>T ENSP00000459592.2:n.*105G>T
ENST00000293778.10:c.*24-22G>T ENSP00000293778.6:n.*24-22G>T
ENST00000574412.5:c.*105G>T ENSP00000459592.1:n.*105G>T
ENST00000576153.5:n.580-22G>T
NM_022059.3:c.*24-22G>T NP_071342.2:n.*24-22G>T
NM_022059.4:c.*24-22G>T NP_071342.2:n.*24-22G>T
NM_001386809.1:c.*24-22G>T MANE Select NP_001373738.1:n.*24-22G>T