Canonical Allele Identifier: CA397281502

Gene: CXCL16

Linked Data

• gnomAD v4: 17-4734634-A-G
• MyVariant Identifiers: chr17:g.4637929A>G (hg19) ; chr17:g.4734634A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734634A>G , CM000679.2:g.4734634A>G	GRCh38
NC_000017.10:g.4637929A>G , CM000679.1:g.4637929A>G	GRCh37
NC_000017.9:g.4584678A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.737T>C MANE Select	ENSP00000293778.7:p.Ile246Thr
ENST00000574412.6:c.737T>C	ENSP00000459592.2:p.Ile246Thr
ENST00000293778.10:c.794T>C	ENSP00000293778.6:p.Ile265Thr
ENST00000574412.5:c.794T>C	ENSP00000459592.1:p.Ile265Thr
ENST00000575168.1:n.568T>C
ENST00000576153.5:n.528T>C
NM_001100812.1:c.794T>C	NP_001094282.1:p.Ile265Thr
NM_022059.3:c.794T>C	NP_071342.2:p.Ile265Thr
NM_022059.4:c.794T>C	NP_071342.2:p.Ile265Thr
NM_001100812.2:c.737T>C	NP_001094282.2:p.Ile246Thr
NM_001386809.1:c.737T>C MANE Select	NP_001373738.1:p.Ile246Thr