Canonical Allele Identifier: CA287188424
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs927878135
gnomAD v3: 17-4734423-G-C
gnomAD v4: 17-4734423-G-C
MyVariant Identifiers: chr17:g.4637718G>C (hg19) chr17:g.4734423G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734423G>C , CM000679.2:g.4734423G>C GRCh38
NC_000017.10:g.4637718G>C , CM000679.1:g.4637718G>C GRCh37
NC_000017.9:g.4584467G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*80C>G MANE Select ENSP00000293778.7:n.*80C>G
ENST00000574412.6:c.*183C>G ENSP00000459592.2:n.*183C>G
ENST00000293778.10:c.*80C>G ENSP00000293778.6:n.*80C>G
ENST00000574412.5:c.*183C>G ENSP00000459592.1:n.*183C>G
ENST00000576153.5:n.636C>G
NM_022059.3:c.*80C>G NP_071342.2:n.*80C>G
NM_022059.4:c.*80C>G NP_071342.2:n.*80C>G
NM_001386809.1:c.*80C>G MANE Select NP_001373738.1:n.*80C>G
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