Canonical Allele Identifier: CA397281511

Gene: CXCL16

Linked Data

• gnomAD v4: 17-4734635-T-C
• MyVariant Identifiers: chr17:g.4637930T>C (hg19) ; chr17:g.4734635T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734635T>C , CM000679.2:g.4734635T>C	GRCh38
NC_000017.10:g.4637930T>C , CM000679.1:g.4637930T>C	GRCh37
NC_000017.9:g.4584679T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.736A>G MANE Select	ENSP00000293778.7:p.Ile246Val
ENST00000574412.6:c.736A>G	ENSP00000459592.2:p.Ile246Val
ENST00000293778.10:c.793A>G	ENSP00000293778.6:p.Ile265Val
ENST00000574412.5:c.793A>G	ENSP00000459592.1:p.Ile265Val
ENST00000575168.1:n.567A>G
ENST00000576153.5:n.527A>G
NM_001100812.1:c.793A>G	NP_001094282.1:p.Ile265Val
NM_022059.3:c.793A>G	NP_071342.2:p.Ile265Val
NM_022059.4:c.793A>G	NP_071342.2:p.Ile265Val
NM_001100812.2:c.736A>G	NP_001094282.2:p.Ile246Val
NM_001386809.1:c.736A>G MANE Select	NP_001373738.1:p.Ile246Val