Canonical Allele Identifier: CA2244533819
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1916088481
gnomAD v4: 17-4734413-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734413A>G , CM000679.2:g.4734413A>G GRCh38
NC_000017.10:g.4637708A>G , CM000679.1:g.4637708A>G GRCh37
NC_000017.9:g.4584457A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*90T>C MANE Select ENSP00000293778.7:n.*90T>C
ENST00000574412.6:c.*193T>C ENSP00000459592.2:n.*193T>C
ENST00000293778.10:c.*90T>C ENSP00000293778.6:n.*90T>C
ENST00000574412.5:c.*193T>C ENSP00000459592.1:n.*193T>C
ENST00000576153.5:n.646T>C
NM_022059.3:c.*90T>C NP_071342.2:n.*90T>C
NM_022059.4:c.*90T>C NP_071342.2:n.*90T>C
NM_001386809.1:c.*90T>C MANE Select NP_001373738.1:n.*90T>C