Canonical Allele Identifier: CA2244533834
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1916088645
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734418A>G , CM000679.2:g.4734418A>G GRCh38
NC_000017.10:g.4637713A>G , CM000679.1:g.4637713A>G GRCh37
NC_000017.9:g.4584462A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293778.12:c.*85T>C MANE Select ENSP00000293778.7:n.*85T>C
ENST00000574412.6:c.*188T>C ENSP00000459592.2:n.*188T>C
ENST00000293778.10:c.*85T>C ENSP00000293778.6:n.*85T>C
ENST00000574412.5:c.*188T>C ENSP00000459592.1:n.*188T>C
ENST00000576153.5:n.641T>C
NM_022059.3:c.*85T>C NP_071342.2:n.*85T>C
NM_022059.4:c.*85T>C NP_071342.2:n.*85T>C
NM_001386809.1:c.*85T>C MANE Select NP_001373738.1:n.*85T>C
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