Canonical Allele Identifier: CA2244533312
Gene: CXCL16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734067G= , CM000679.2:g.4734067G= GRCh38
NC_000017.10:g.4637362G= , CM000679.1:g.4637362G= GRCh37
NC_000017.9:g.4584111G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*436C= MANE Select ENSP00000293778.7:n.*436C=
ENST00000293778.10:c.*436C= ENSP00000293778.6:n.*436C=
ENST00000576153.5:n.992C=
NM_022059.3:c.*436C= NP_071342.2:n.*436C=
NM_022059.4:c.*436C= NP_071342.2:n.*436C=
NM_001386809.1:c.*436C= MANE Select NP_001373738.1:n.*436C=