Canonical Allele Identifier: CA624612293

Gene: CXCL16

Linked Data

• dbSNP Id: rs1281759947
• gnomAD v2: 17-4637724-A-G
• gnomAD v3: 17-4734429-A-G
• gnomAD v4: 17-4734429-A-G
• MyVariant Identifiers: chr17:g.4637724A>G (hg19) ; chr17:g.4734429A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734429A>G , CM000679.2:g.4734429A>G	GRCh38
NC_000017.10:g.4637724A>G , CM000679.1:g.4637724A>G	GRCh37
NC_000017.9:g.4584473A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*74T>C MANE Select	ENSP00000293778.7:n.*74T>C
ENST00000574412.6:c.*177T>C	ENSP00000459592.2:n.*177T>C
ENST00000293778.10:c.*74T>C	ENSP00000293778.6:n.*74T>C
ENST00000574412.5:c.*177T>C	ENSP00000459592.1:n.*177T>C
ENST00000576153.5:n.630T>C
NM_022059.3:c.*74T>C	NP_071342.2:n.*74T>C
NM_022059.4:c.*74T>C	NP_071342.2:n.*74T>C
NM_001386809.1:c.*74T>C MANE Select	NP_001373738.1:n.*74T>C