Canonical Allele Identifier: CA2635550107
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734408-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734408T>A , CM000679.2:g.4734408T>A GRCh38
NC_000017.10:g.4637703T>A , CM000679.1:g.4637703T>A GRCh37
NC_000017.9:g.4584452T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*95A>T MANE Select ENSP00000293778.7:n.*95A>T
ENST00000574412.6:c.*198A>T ENSP00000459592.2:n.*198A>T
ENST00000293778.10:c.*95A>T ENSP00000293778.6:n.*95A>T
ENST00000574412.5:c.*198A>T ENSP00000459592.1:n.*198A>T
ENST00000576153.5:n.651A>T
NM_022059.3:c.*95A>T NP_071342.2:n.*95A>T
NM_022059.4:c.*95A>T NP_071342.2:n.*95A>T
NM_001386809.1:c.*95A>T MANE Select NP_001373738.1:n.*95A>T