Canonical Allele Identifier: CA772506997
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1454408504
gnomAD v3: 17-4734315-C-G
gnomAD v4: 17-4734315-C-G
MyVariant Identifiers: chr17:g.4637610C>G (hg19) chr17:g.4734315C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734315C>G , CM000679.2:g.4734315C>G GRCh38
NC_000017.10:g.4637610C>G , CM000679.1:g.4637610C>G GRCh37
NC_000017.9:g.4584359C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*188G>C MANE Select ENSP00000293778.7:n.*188G>C
ENST00000574412.6:c.*291G>C ENSP00000459592.2:n.*291G>C
ENST00000293778.10:c.*188G>C ENSP00000293778.6:n.*188G>C
ENST00000574412.5:c.*291G>C ENSP00000459592.1:n.*291G>C
ENST00000576153.5:n.744G>C
NM_022059.3:c.*188G>C NP_071342.2:n.*188G>C
NM_022059.4:c.*188G>C NP_071342.2:n.*188G>C
NM_001386809.1:c.*188G>C MANE Select NP_001373738.1:n.*188G>C
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