Canonical Allele Identifier: CA2635549990
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734268-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734268A>G , CM000679.2:g.4734268A>G GRCh38
NC_000017.10:g.4637563A>G , CM000679.1:g.4637563A>G GRCh37
NC_000017.9:g.4584312A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*235T>C MANE Select ENSP00000293778.7:n.*235T>C
ENST00000293778.10:c.*235T>C ENSP00000293778.6:n.*235T>C
ENST00000576153.5:n.791T>C
NM_022059.3:c.*235T>C NP_071342.2:n.*235T>C
NM_022059.4:c.*235T>C NP_071342.2:n.*235T>C
NM_001386809.1:c.*235T>C MANE Select NP_001373738.1:n.*235T>C
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