Canonical Allele Identifier: CA2244534125
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1051009

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734591G>C , CM000679.2:g.4734591G>C GRCh38
NC_000017.10:g.4637886G>C , CM000679.1:g.4637886G>C GRCh37
NC_000017.9:g.4584635G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293778.12:c.*15C>G MANE Select ENSP00000293778.7:n.*15C>G
ENST00000574412.6:c.*15C>G ENSP00000459592.2:n.*15C>G
ENST00000293778.10:c.*15C>G ENSP00000293778.6:n.*15C>G
ENST00000574412.5:c.*15C>G ENSP00000459592.1:n.*15C>G
ENST00000575168.1:n.611C>G
ENST00000576153.5:n.571C>G
NM_001100812.1:c.*15C>G NP_001094282.1:n.*15C>G
NM_022059.3:c.*15C>G NP_071342.2:n.*15C>G
NM_022059.4:c.*15C>G NP_071342.2:n.*15C>G
NM_001100812.2:c.*15C>G NP_001094282.2:n.*15C>G
NM_001386809.1:c.*15C>G MANE Select NP_001373738.1:n.*15C>G