Canonical Allele Identifier: CA2244533350
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734101C= , CM000679.2:g.4734101C= GRCh38
NC_000017.10:g.4637396C= , CM000679.1:g.4637396C= GRCh37
NC_000017.9:g.4584145C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*402G= MANE Select ENSP00000293778.7:n.*402G=
ENST00000293778.10:c.*402G= ENSP00000293778.6:n.*402G=
ENST00000576153.5:n.958G=
NM_022059.3:c.*402G= NP_071342.2:n.*402G=
NM_022059.4:c.*402G= NP_071342.2:n.*402G=
NM_001386809.1:c.*402G= MANE Select NP_001373738.1:n.*402G=