Canonical Allele Identifier: CA2635549608
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734053-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734053C>A , CM000679.2:g.4734053C>A GRCh38
NC_000017.10:g.4637348C>A , CM000679.1:g.4637348C>A GRCh37
NC_000017.9:g.4584097C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*450G>T MANE Select ENSP00000293778.7:n.*450G>T
ENST00000293778.10:c.*450G>T ENSP00000293778.6:n.*450G>T
ENST00000576153.5:n.1006G>T
NM_022059.3:c.*450G>T NP_071342.2:n.*450G>T
NM_022059.4:c.*450G>T NP_071342.2:n.*450G>T
NM_001386809.1:c.*450G>T MANE Select NP_001373738.1:n.*450G>T