Canonical Allele Identifier: CA2244533231

Gene: CXCL16

Linked Data

• dbSNP Id: rs1916075148

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734025T>C , CM000679.2:g.4734025T>C	GRCh38
NC_000017.10:g.4637320T>C , CM000679.1:g.4637320T>C	GRCh37
NC_000017.9:g.4584069T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*478A>G MANE Select	ENSP00000293778.7:n.*478A>G
ENST00000293778.10:c.*478A>G	ENSP00000293778.6:n.*478A>G
ENST00000576153.5:n.1034A>G
NM_022059.3:c.*478A>G	NP_071342.2:n.*478A>G
NM_022059.4:c.*478A>G	NP_071342.2:n.*478A>G
NM_001386809.1:c.*478A>G MANE Select	NP_001373738.1:n.*478A>G