Canonical Allele Identifier: CA287188483

Gene: CXCL16

Linked Data

• dbSNP Id: rs1031560882
• gnomAD v3: 17-4734523-C-T
• gnomAD v4: 17-4734523-C-T
• MyVariant Identifiers: chr17:g.4637818C>T (hg19) ; chr17:g.4734523C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734523C>T , CM000679.2:g.4734523C>T	GRCh38
NC_000017.10:g.4637818C>T , CM000679.1:g.4637818C>T	GRCh37
NC_000017.9:g.4584567C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000293778.12:c.*24-44G>A MANE Select	ENSP00000293778.7:n.*24-44G>A
ENST00000574412.6:c.*83G>A	ENSP00000459592.2:n.*83G>A
ENST00000293778.10:c.*24-44G>A	ENSP00000293778.6:n.*24-44G>A
ENST00000574412.5:c.*83G>A	ENSP00000459592.1:n.*83G>A
ENST00000576153.5:n.580-44G>A
NM_001100812.1:c.*83G>A	NP_001094282.1:n.*83G>A
NM_022059.3:c.*24-44G>A	NP_071342.2:n.*24-44G>A
NM_022059.4:c.*24-44G>A	NP_071342.2:n.*24-44G>A
NM_001100812.2:c.*83G>A	NP_001094282.2:n.*83G>A
NM_001386809.1:c.*24-44G>A MANE Select	NP_001373738.1:n.*24-44G>A