Canonical Allele Identifier: CA2635550054
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734335-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734335G>C , CM000679.2:g.4734335G>C GRCh38
NC_000017.10:g.4637630G>C , CM000679.1:g.4637630G>C GRCh37
NC_000017.9:g.4584379G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*168C>G MANE Select ENSP00000293778.7:n.*168C>G
ENST00000574412.6:c.*271C>G ENSP00000459592.2:n.*271C>G
ENST00000293778.10:c.*168C>G ENSP00000293778.6:n.*168C>G
ENST00000574412.5:c.*271C>G ENSP00000459592.1:n.*271C>G
ENST00000576153.5:n.724C>G
NM_022059.3:c.*168C>G NP_071342.2:n.*168C>G
NM_022059.4:c.*168C>G NP_071342.2:n.*168C>G
NM_001386809.1:c.*168C>G MANE Select NP_001373738.1:n.*168C>G
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