Canonical Allele Identifier: CA980962365

Gene: CXCL16

Linked Data

• dbSNP Id: rs1025609407
• gnomAD v3: 17-4734553-C-A
• gnomAD v4: 17-4734553-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734553C>A , CM000679.2:g.4734553C>A	GRCh38
NC_000017.10:g.4637848C>A , CM000679.1:g.4637848C>A	GRCh37
NC_000017.9:g.4584597C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*23+30G>T MANE Select	ENSP00000293778.7:n.*23+30G>T
ENST00000574412.6:c.*53G>T	ENSP00000459592.2:n.*53G>T
ENST00000293778.10:c.*23+30G>T	ENSP00000293778.6:n.*23+30G>T
ENST00000574412.5:c.*53G>T	ENSP00000459592.1:n.*53G>T
ENST00000576153.5:n.579+30G>T
NM_001100812.1:c.*53G>T	NP_001094282.1:n.*53G>T
NM_022059.3:c.*23+30G>T	NP_071342.2:n.*23+30G>T
NM_022059.4:c.*23+30G>T	NP_071342.2:n.*23+30G>T
NM_001100812.2:c.*53G>T	NP_001094282.2:n.*53G>T
NM_001386809.1:c.*23+30G>T MANE Select	NP_001373738.1:n.*23+30G>T