Canonical Allele Identifier: CA980962037

Gene: CXCL16

Linked Data

• dbSNP Id: rs1916078274
• gnomAD v3: 17-4734102-A-G
• gnomAD v4: 17-4734102-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734102A>G , CM000679.2:g.4734102A>G	GRCh38
NC_000017.10:g.4637397A>G , CM000679.1:g.4637397A>G	GRCh37
NC_000017.9:g.4584146A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*401T>C MANE Select	ENSP00000293778.7:n.*401T>C
ENST00000293778.10:c.*401T>C	ENSP00000293778.6:n.*401T>C
ENST00000576153.5:n.957T>C
NM_022059.3:c.*401T>C	NP_071342.2:n.*401T>C
NM_022059.4:c.*401T>C	NP_071342.2:n.*401T>C
NM_001386809.1:c.*401T>C MANE Select	NP_001373738.1:n.*401T>C