Canonical Allele Identifier: CA772507136

Gene: CXCL16

Linked Data

• dbSNP Id: rs1276706936
• MyVariant Identifiers: chr17:g.4637876A>G (hg19) ; chr17:g.4734581A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734581A>G , CM000679.2:g.4734581A>G	GRCh38
NC_000017.10:g.4637876A>G , CM000679.1:g.4637876A>G	GRCh37
NC_000017.9:g.4584625A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*23+2T>C MANE Select	ENSP00000293778.7:n.*23+2T>C
ENST00000574412.6:c.*25T>C	ENSP00000459592.2:n.*25T>C
ENST00000293778.10:c.*23+2T>C	ENSP00000293778.6:n.*23+2T>C
ENST00000574412.5:c.*25T>C	ENSP00000459592.1:n.*25T>C
ENST00000576153.5:n.579+2T>C
NM_001100812.1:c.*25T>C	NP_001094282.1:n.*25T>C
NM_022059.3:c.*23+2T>C	NP_071342.2:n.*23+2T>C
NM_022059.4:c.*23+2T>C	NP_071342.2:n.*23+2T>C
NM_001100812.2:c.*25T>C	NP_001094282.2:n.*25T>C
NM_001386809.1:c.*23+2T>C MANE Select	NP_001373738.1:n.*23+2T>C