Canonical Allele Identifier: CA2635550130
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734426-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734426A>G , CM000679.2:g.4734426A>G GRCh38
NC_000017.10:g.4637721A>G , CM000679.1:g.4637721A>G GRCh37
NC_000017.9:g.4584470A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*77T>C MANE Select ENSP00000293778.7:n.*77T>C
ENST00000574412.6:c.*180T>C ENSP00000459592.2:n.*180T>C
ENST00000293778.10:c.*77T>C ENSP00000293778.6:n.*77T>C
ENST00000574412.5:c.*180T>C ENSP00000459592.1:n.*180T>C
ENST00000576153.5:n.633T>C
NM_022059.3:c.*77T>C NP_071342.2:n.*77T>C
NM_022059.4:c.*77T>C NP_071342.2:n.*77T>C
NM_001386809.1:c.*77T>C MANE Select NP_001373738.1:n.*77T>C