Canonical Allele Identifier: CA2244534028
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1597497655
gnomAD v4: 17-4734515-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734515G>A , CM000679.2:g.4734515G>A GRCh38
NC_000017.10:g.4637810G>A , CM000679.1:g.4637810G>A GRCh37
NC_000017.9:g.4584559G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*24-36C>T MANE Select ENSP00000293778.7:n.*24-36C>T
ENST00000574412.6:c.*91C>T ENSP00000459592.2:n.*91C>T
ENST00000293778.10:c.*24-36C>T ENSP00000293778.6:n.*24-36C>T
ENST00000574412.5:c.*91C>T ENSP00000459592.1:n.*91C>T
ENST00000576153.5:n.580-36C>T
NM_001100812.1:c.*91C>T NP_001094282.1:n.*91C>T
NM_022059.3:c.*24-36C>T NP_071342.2:n.*24-36C>T
NM_022059.4:c.*24-36C>T NP_071342.2:n.*24-36C>T
NM_001100812.2:c.*91C>T NP_001094282.2:n.*91C>T
NM_001386809.1:c.*24-36C>T MANE Select NP_001373738.1:n.*24-36C>T