Canonical Allele Identifier: CA8309119

Gene: CXCL16

Linked Data

• dbSNP Id: rs749396444
• ExAC: 17:4637920 G / A
• gnomAD v2: 17-4637920-G-A
• gnomAD v3: 17-4734625-G-A
• gnomAD v4: 17-4734625-G-A
• MyVariant Identifiers: chr17:g.4637920G>A (hg19) ; chr17:g.4734625G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734625G>A , CM000679.2:g.4734625G>A	GRCh38
NC_000017.10:g.4637920G>A , CM000679.1:g.4637920G>A	GRCh37
NC_000017.9:g.4584669G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.746C>T MANE Select	ENSP00000293778.7:p.Ala249Val
ENST00000574412.6:c.746C>T	ENSP00000459592.2:p.Ala249Val
ENST00000293778.10:c.803C>T	ENSP00000293778.6:p.Ala268Val
ENST00000574412.5:c.803C>T	ENSP00000459592.1:p.Ala268Val
ENST00000575168.1:n.577C>T
ENST00000576153.5:n.537C>T
NM_001100812.1:c.803C>T	NP_001094282.1:p.Ala268Val
NM_022059.3:c.803C>T	NP_071342.2:p.Ala268Val
NM_022059.4:c.803C>T	NP_071342.2:p.Ala268Val
NM_001100812.2:c.746C>T	NP_001094282.2:p.Ala249Val
NM_001386809.1:c.746C>T MANE Select	NP_001373738.1:p.Ala249Val