Canonical Allele Identifier: CA2635550144

Gene: CXCL16

Linked Data

• gnomAD v4: 17-4734439-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4734439T>C , CM000679.2:g.4734439T>C	GRCh38
NC_000017.10:g.4637734T>C , CM000679.1:g.4637734T>C	GRCh37
NC_000017.9:g.4584483T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000293778.12:c.*64A>G MANE Select	ENSP00000293778.7:n.*64A>G
ENST00000574412.6:c.*167A>G	ENSP00000459592.2:n.*167A>G
ENST00000293778.10:c.*64A>G	ENSP00000293778.6:n.*64A>G
ENST00000574412.5:c.*167A>G	ENSP00000459592.1:n.*167A>G
ENST00000576153.5:n.620A>G
NM_022059.3:c.*64A>G	NP_071342.2:n.*64A>G
NM_022059.4:c.*64A>G	NP_071342.2:n.*64A>G
NM_001386809.1:c.*64A>G MANE Select	NP_001373738.1:n.*64A>G