Canonical Allele Identifier: CA2635550000
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734277-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734277A>C , CM000679.2:g.4734277A>C GRCh38
NC_000017.10:g.4637572A>C , CM000679.1:g.4637572A>C GRCh37
NC_000017.9:g.4584321A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*226T>G MANE Select ENSP00000293778.7:n.*226T>G
ENST00000293778.10:c.*226T>G ENSP00000293778.6:n.*226T>G
ENST00000576153.5:n.782T>G
NM_022059.3:c.*226T>G NP_071342.2:n.*226T>G
NM_022059.4:c.*226T>G NP_071342.2:n.*226T>G
NM_001386809.1:c.*226T>G MANE Select NP_001373738.1:n.*226T>G