Canonical Allele Identifier: CA2635550261
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734532-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734532A>G , CM000679.2:g.4734532A>G GRCh38
NC_000017.10:g.4637827A>G , CM000679.1:g.4637827A>G GRCh37
NC_000017.9:g.4584576A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293778.12:c.*23+51T>C MANE Select ENSP00000293778.7:n.*23+51T>C
ENST00000574412.6:c.*74T>C ENSP00000459592.2:n.*74T>C
ENST00000293778.10:c.*23+51T>C ENSP00000293778.6:n.*23+51T>C
ENST00000574412.5:c.*74T>C ENSP00000459592.1:n.*74T>C
ENST00000576153.5:n.579+51T>C
NM_001100812.1:c.*74T>C NP_001094282.1:n.*74T>C
NM_022059.3:c.*23+51T>C NP_071342.2:n.*23+51T>C
NM_022059.4:c.*23+51T>C NP_071342.2:n.*23+51T>C
NM_001100812.2:c.*74T>C NP_001094282.2:n.*74T>C
NM_001386809.1:c.*23+51T>C MANE Select NP_001373738.1:n.*23+51T>C
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