Canonical Allele Identifier: CA2635549976
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734251-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734251C>T , CM000679.2:g.4734251C>T GRCh38
NC_000017.10:g.4637546C>T , CM000679.1:g.4637546C>T GRCh37
NC_000017.9:g.4584295C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*252G>A MANE Select ENSP00000293778.7:n.*252G>A
ENST00000293778.10:c.*252G>A ENSP00000293778.6:n.*252G>A
ENST00000576153.5:n.808G>A
NM_022059.3:c.*252G>A NP_071342.2:n.*252G>A
NM_022059.4:c.*252G>A NP_071342.2:n.*252G>A
NM_001386809.1:c.*252G>A MANE Select NP_001373738.1:n.*252G>A
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