Canonical Allele Identifier: CA8309133

Gene: CXCL16

Linked Data

• dbSNP Id: rs759191861
• ExAC: 17:4637969 A / G
• gnomAD v2: 17-4637969-A-G
• gnomAD v3: 17-4734674-A-G
• gnomAD v4: 17-4734674-A-G
• MyVariant Identifiers: chr17:g.4637969A>G (hg19) ; chr17:g.4734674A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734674A>G , CM000679.2:g.4734674A>G	GRCh38
NC_000017.10:g.4637969A>G , CM000679.1:g.4637969A>G	GRCh37
NC_000017.9:g.4584718A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.719-22T>C MANE Select	ENSP00000293778.7:n.719-22T>C
ENST00000574412.6:c.719-22T>C	ENSP00000459592.2:n.719-22T>C
ENST00000293778.10:c.776-22T>C	ENSP00000293778.6:n.776-22T>C
ENST00000574412.5:c.776-22T>C	ENSP00000459592.1:n.776-22T>C
ENST00000575168.1:n.550-22T>C
ENST00000576153.5:n.510-22T>C
NM_001100812.1:c.776-22T>C	NP_001094282.1:n.776-22T>C
NM_022059.3:c.776-22T>C	NP_071342.2:n.776-22T>C
NM_022059.4:c.776-22T>C	NP_071342.2:n.776-22T>C
NM_001100812.2:c.719-22T>C	NP_001094282.2:n.719-22T>C
NM_001386809.1:c.719-22T>C MANE Select	NP_001373738.1:n.719-22T>C