Canonical Allele Identifier: CA287188183
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs200241400
gnomAD v2: 17-4637331-C-CG
gnomAD v3: 17-4734036-C-CG
gnomAD v4: 17-4734036-C-CG
MyVariant Identifiers: chr17:g.4637331_4637332insG (hg19) chr17:g.4734036_4734037insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734037dup , CM000679.2:g.4734037dup GRCh38
NC_000017.10:g.4637332dup , CM000679.1:g.4637332dup GRCh37
NC_000017.9:g.4584081dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*466dup MANE Select ENSP00000293778.7:n.*466dup
ENST00000293778.10:c.*466dup ENSP00000293778.6:n.*466dup
ENST00000576153.5:n.1022dup
NM_022059.3:c.*466dup NP_071342.2:n.*466dup
NM_022059.4:c.*466dup NP_071342.2:n.*466dup
NM_001386809.1:c.*466dup MANE Select NP_001373738.1:n.*466dup
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Search 100 bp 3'