Canonical Allele Identifier: CA2635550109

Gene: CXCL16

Linked Data

• gnomAD v4: 17-4734411-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734411A>C , CM000679.2:g.4734411A>C	GRCh38
NC_000017.10:g.4637706A>C , CM000679.1:g.4637706A>C	GRCh37
NC_000017.9:g.4584455A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000293778.12:c.*92T>G MANE Select	ENSP00000293778.7:n.*92T>G
ENST00000574412.6:c.*195T>G	ENSP00000459592.2:n.*195T>G
ENST00000293778.10:c.*92T>G	ENSP00000293778.6:n.*92T>G
ENST00000574412.5:c.*195T>G	ENSP00000459592.1:n.*195T>G
ENST00000576153.5:n.648T>G
NM_022059.3:c.*92T>G	NP_071342.2:n.*92T>G
NM_022059.4:c.*92T>G	NP_071342.2:n.*92T>G
NM_001386809.1:c.*92T>G MANE Select	NP_001373738.1:n.*92T>G