Canonical Allele Identifier: CA2635550588
Gene: CXCL16 HGNC NCBI

Linked Data

gnomAD v4: 17-4734757-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734757C>T , CM000679.2:g.4734757C>T GRCh38
NC_000017.10:g.4638052C>T , CM000679.1:g.4638052C>T GRCh37
NC_000017.9:g.4584801C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.719-105G>A MANE Select ENSP00000293778.7:n.719-105G>A
ENST00000574412.6:c.719-105G>A ENSP00000459592.2:n.719-105G>A
ENST00000293778.10:c.776-105G>A ENSP00000293778.6:n.776-105G>A
ENST00000574412.5:c.776-105G>A ENSP00000459592.1:n.776-105G>A
ENST00000575168.1:n.550-105G>A
ENST00000576153.5:n.510-105G>A
NM_001100812.1:c.776-105G>A NP_001094282.1:n.776-105G>A
NM_022059.3:c.776-105G>A NP_071342.2:n.776-105G>A
NM_022059.4:c.776-105G>A NP_071342.2:n.776-105G>A
NM_001100812.2:c.719-105G>A NP_001094282.2:n.719-105G>A
NM_001386809.1:c.719-105G>A MANE Select NP_001373738.1:n.719-105G>A
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