Canonical Allele Identifier: CA772507108

Gene: CXCL16

Linked Data

• dbSNP Id: rs1168858979
• MyVariant Identifiers: chr17:g.4637811T>C (hg19) ; chr17:g.4734516T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734516T>C , CM000679.2:g.4734516T>C	GRCh38
NC_000017.10:g.4637811T>C , CM000679.1:g.4637811T>C	GRCh37
NC_000017.9:g.4584560T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*24-37A>G MANE Select	ENSP00000293778.7:n.*24-37A>G
ENST00000574412.6:c.*90A>G	ENSP00000459592.2:n.*90A>G
ENST00000293778.10:c.*24-37A>G	ENSP00000293778.6:n.*24-37A>G
ENST00000574412.5:c.*90A>G	ENSP00000459592.1:n.*90A>G
ENST00000576153.5:n.580-37A>G
NM_001100812.1:c.*90A>G	NP_001094282.1:n.*90A>G
NM_022059.3:c.*24-37A>G	NP_071342.2:n.*24-37A>G
NM_022059.4:c.*24-37A>G	NP_071342.2:n.*24-37A>G
NM_001100812.2:c.*90A>G	NP_001094282.2:n.*90A>G
NM_001386809.1:c.*24-37A>G MANE Select	NP_001373738.1:n.*24-37A>G