Canonical Allele Identifier: CA287188686

Gene: CXCL16

Linked Data

• dbSNP Id: rs556829982
• gnomAD v3: 17-4734721-G-A
• gnomAD v4: 17-4734721-G-A
• MyVariant Identifiers: chr17:g.4638016G>A (hg19) ; chr17:g.4734721G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734721G>A , CM000679.2:g.4734721G>A	GRCh38
NC_000017.10:g.4638016G>A , CM000679.1:g.4638016G>A	GRCh37
NC_000017.9:g.4584765G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.719-69C>T MANE Select	ENSP00000293778.7:n.719-69C>T
ENST00000574412.6:c.719-69C>T	ENSP00000459592.2:n.719-69C>T
ENST00000293778.10:c.776-69C>T	ENSP00000293778.6:n.776-69C>T
ENST00000574412.5:c.776-69C>T	ENSP00000459592.1:n.776-69C>T
ENST00000575168.1:n.550-69C>T
ENST00000576153.5:n.510-69C>T
NM_001100812.1:c.776-69C>T	NP_001094282.1:n.776-69C>T
NM_022059.3:c.776-69C>T	NP_071342.2:n.776-69C>T
NM_022059.4:c.776-69C>T	NP_071342.2:n.776-69C>T
NM_001100812.2:c.719-69C>T	NP_001094282.2:n.719-69C>T
NM_001386809.1:c.719-69C>T MANE Select	NP_001373738.1:n.719-69C>T