Canonical Allele Identifier: CA287188487

Gene: CXCL16

Linked Data

• dbSNP Id: rs373758483
• gnomAD v4: 17-4734537-T-A
• MyVariant Identifiers: chr17:g.4637832T>A (hg19) ; chr17:g.4734537T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734537T>A , CM000679.2:g.4734537T>A	GRCh38
NC_000017.10:g.4637832T>A , CM000679.1:g.4637832T>A	GRCh37
NC_000017.9:g.4584581T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*23+46A>T MANE Select	ENSP00000293778.7:n.*23+46A>T
ENST00000574412.6:c.*69A>T	ENSP00000459592.2:n.*69A>T
ENST00000293778.10:c.*23+46A>T	ENSP00000293778.6:n.*23+46A>T
ENST00000574412.5:c.*69A>T	ENSP00000459592.1:n.*69A>T
ENST00000576153.5:n.579+46A>T
NM_001100812.1:c.*69A>T	NP_001094282.1:n.*69A>T
NM_022059.3:c.*23+46A>T	NP_071342.2:n.*23+46A>T
NM_022059.4:c.*23+46A>T	NP_071342.2:n.*23+46A>T
NM_001100812.2:c.*69A>T	NP_001094282.2:n.*69A>T
NM_001386809.1:c.*23+46A>T MANE Select	NP_001373738.1:n.*23+46A>T