Canonical Allele Identifier: CA2244533485
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734192C= , CM000679.2:g.4734192C= GRCh38
NC_000017.10:g.4637487C= , CM000679.1:g.4637487C= GRCh37
NC_000017.9:g.4584236C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*311G= MANE Select ENSP00000293778.7:n.*311G=
ENST00000293778.10:c.*311G= ENSP00000293778.6:n.*311G=
ENST00000576153.5:n.867G=
NM_022059.3:c.*311G= NP_071342.2:n.*311G=
NM_022059.4:c.*311G= NP_071342.2:n.*311G=
NM_001386809.1:c.*311G= MANE Select NP_001373738.1:n.*311G=