Canonical Allele Identifier: CA772507109
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1467475041
MyVariant Identifiers: chr17:g.4637814C>G (hg19) chr17:g.4734519C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734519C>G , CM000679.2:g.4734519C>G GRCh38
NC_000017.10:g.4637814C>G , CM000679.1:g.4637814C>G GRCh37
NC_000017.9:g.4584563C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*24-40G>C MANE Select ENSP00000293778.7:n.*24-40G>C
ENST00000574412.6:c.*87G>C ENSP00000459592.2:n.*87G>C
ENST00000293778.10:c.*24-40G>C ENSP00000293778.6:n.*24-40G>C
ENST00000574412.5:c.*87G>C ENSP00000459592.1:n.*87G>C
ENST00000576153.5:n.580-40G>C
NM_001100812.1:c.*87G>C NP_001094282.1:n.*87G>C
NM_022059.3:c.*24-40G>C NP_071342.2:n.*24-40G>C
NM_022059.4:c.*24-40G>C NP_071342.2:n.*24-40G>C
NM_001100812.2:c.*87G>C NP_001094282.2:n.*87G>C
NM_001386809.1:c.*24-40G>C MANE Select NP_001373738.1:n.*24-40G>C
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