Canonical Allele Identifier: CA287188275
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs546492148
gnomAD v2: 17-4637395-T-G
gnomAD v3: 17-4734100-T-G
gnomAD v4: 17-4734100-T-G
MyVariant Identifiers: chr17:g.4637395T>G (hg19) chr17:g.4734100T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734100T>G , CM000679.2:g.4734100T>G GRCh38
NC_000017.10:g.4637395T>G , CM000679.1:g.4637395T>G GRCh37
NC_000017.9:g.4584144T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*403A>C MANE Select ENSP00000293778.7:n.*403A>C
ENST00000293778.10:c.*403A>C ENSP00000293778.6:n.*403A>C
ENST00000576153.5:n.959A>C
NM_022059.3:c.*403A>C NP_071342.2:n.*403A>C
NM_022059.4:c.*403A>C NP_071342.2:n.*403A>C
NM_001386809.1:c.*403A>C MANE Select NP_001373738.1:n.*403A>C
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