Canonical Allele Identifier: CA2635550022
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734297-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734297C>A , CM000679.2:g.4734297C>A GRCh38
NC_000017.10:g.4637592C>A , CM000679.1:g.4637592C>A GRCh37
NC_000017.9:g.4584341C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*206G>T MANE Select ENSP00000293778.7:n.*206G>T
ENST00000574412.6:c.*309G>T ENSP00000459592.2:n.*309G>T
ENST00000293778.10:c.*206G>T ENSP00000293778.6:n.*206G>T
ENST00000574412.5:c.*309G>T ENSP00000459592.1:n.*309G>T
ENST00000576153.5:n.762G>T
NM_022059.3:c.*206G>T NP_071342.2:n.*206G>T
NM_022059.4:c.*206G>T NP_071342.2:n.*206G>T
NM_001386809.1:c.*206G>T MANE Select NP_001373738.1:n.*206G>T
Search 100 bp 5'
Search 100 bp 3'