Canonical Allele Identifier: CA8309112
Gene: CXCL16 HGNC NCBI
COSMIC:
COSN165307 (not active)
COSN6657557 (not active)
MyVariant.info:
GRCh38 chr17:g.4734591G>A
GRCh37 chr17:g.4637886G>A
gnomAD v2:
17:4637886 G / A
gnomAD v3:
17:4734591 G / A
gnomAD v4:
chr17-4734591-G-A
Joint Max Group AF 0.49168725 (EAS)
Genomes Max Group AF 0.49173697 (EAS)
Exomes Max Group AF 0.48994266 (EAS)
dbSNP:
1051009
JSON-LD

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
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