Canonical Allele Identifier: CA2244533903

Gene: CXCL16

Linked Data

• dbSNP Id: rs1916090538

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734468T>G , CM000679.2:g.4734468T>G	GRCh38
NC_000017.10:g.4637763T>G , CM000679.1:g.4637763T>G	GRCh37
NC_000017.9:g.4584512T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*35A>C MANE Select	ENSP00000293778.7:n.*35A>C
ENST00000574412.6:c.*138A>C	ENSP00000459592.2:n.*138A>C
ENST00000293778.10:c.*35A>C	ENSP00000293778.6:n.*35A>C
ENST00000574412.5:c.*138A>C	ENSP00000459592.1:n.*138A>C
ENST00000576153.5:n.591A>C
NM_022059.3:c.*35A>C	NP_071342.2:n.*35A>C
NM_022059.4:c.*35A>C	NP_071342.2:n.*35A>C
NM_001386809.1:c.*35A>C MANE Select	NP_001373738.1:n.*35A>C