Canonical Allele Identifier: CA8309112

Gene: CXCL16

Linked Data

• dbSNP Id: rs1051009
• ExAC: 17:4637886 G / A
• gnomAD v2: 17-4637886-G-A
• gnomAD v3: 17-4734591-G-A
• gnomAD v4: 17-4734591-G-A
• MyVariant Identifiers: chr17:g.4637886G>A (hg19) ; chr17:g.4734591G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734591G>A , CM000679.2:g.4734591G>A	GRCh38
NC_000017.10:g.4637886G>A , CM000679.1:g.4637886G>A	GRCh37
NC_000017.9:g.4584635G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000293778.12:c.*15C>T MANE Select	ENSP00000293778.7:n.*15C>T
ENST00000574412.6:c.*15C>T	ENSP00000459592.2:n.*15C>T
ENST00000293778.10:c.*15C>T	ENSP00000293778.6:n.*15C>T
ENST00000574412.5:c.*15C>T	ENSP00000459592.1:n.*15C>T
ENST00000575168.1:n.611C>T
ENST00000576153.5:n.571C>T
NM_001100812.1:c.*15C>T	NP_001094282.1:n.*15C>T
NM_022059.3:c.*15C>T	NP_071342.2:n.*15C>T
NM_022059.4:c.*15C>T	NP_071342.2:n.*15C>T
NM_001100812.2:c.*15C>T	NP_001094282.2:n.*15C>T
NM_001386809.1:c.*15C>T MANE Select	NP_001373738.1:n.*15C>T