Canonical Allele Identifier: CA287188409
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs937534855
gnomAD v3: 17-4734402-C-T
gnomAD v4: 17-4734402-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734402C>T , CM000679.2:g.4734402C>T GRCh38
NC_000017.10:g.4637697C>T , CM000679.1:g.4637697C>T GRCh37
NC_000017.9:g.4584446C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*101G>A MANE Select ENSP00000293778.7:n.*101G>A
ENST00000574412.6:c.*204G>A ENSP00000459592.2:n.*204G>A
ENST00000293778.10:c.*101G>A ENSP00000293778.6:n.*101G>A
ENST00000574412.5:c.*204G>A ENSP00000459592.1:n.*204G>A
ENST00000576153.5:n.657G>A
NM_022059.3:c.*101G>A NP_071342.2:n.*101G>A
NM_022059.4:c.*101G>A NP_071342.2:n.*101G>A
NM_001386809.1:c.*101G>A MANE Select NP_001373738.1:n.*101G>A