Canonical Allele Identifier: CA624612353

Gene: CXCL16

Linked Data

• dbSNP Id: rs1163855241
• gnomAD v2: 17-4638096-A-C
• gnomAD v3: 17-4734801-A-C
• gnomAD v4: 17-4734801-A-C
• MyVariant Identifiers: chr17:g.4638096A>C (hg19) ; chr17:g.4734801A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734801A>C , CM000679.2:g.4734801A>C	GRCh38
NC_000017.10:g.4638096A>C , CM000679.1:g.4638096A>C	GRCh37
NC_000017.9:g.4584845A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.719-149T>G MANE Select	ENSP00000293778.7:n.719-149T>G
ENST00000574412.6:c.719-149T>G	ENSP00000459592.2:n.719-149T>G
ENST00000293778.10:c.776-149T>G	ENSP00000293778.6:n.776-149T>G
ENST00000574412.5:c.776-149T>G	ENSP00000459592.1:n.776-149T>G
ENST00000575168.1:n.550-149T>G
ENST00000576153.5:n.510-149T>G
NM_001100812.1:c.776-149T>G	NP_001094282.1:n.776-149T>G
NM_022059.3:c.776-149T>G	NP_071342.2:n.776-149T>G
NM_022059.4:c.776-149T>G	NP_071342.2:n.776-149T>G
NM_001100812.2:c.719-149T>G	NP_001094282.2:n.719-149T>G
NM_001386809.1:c.719-149T>G MANE Select	NP_001373738.1:n.719-149T>G