Canonical Allele Identifier: CA624612212
Gene: CXCL16 HGNC NCBI

Linked Data

dbSNP Id: rs1450446119
gnomAD v2: 17-4637327-A-AT
gnomAD v3: 17-4734032-A-AT
gnomAD v4: 17-4734032-A-AT
MyVariant Identifiers: chr17:g.4637327_4637328insT (hg19) chr17:g.4734032_4734033insT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4734032_4734033insT , CM000679.2:g.4734032_4734033insT GRCh38
NC_000017.10:g.4637327_4637328insT , CM000679.1:g.4637327_4637328insT GRCh37
NC_000017.9:g.4584076_4584077insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293778.12:c.*470_*471insA MANE Select ENSP00000293778.7:n.*470_*471insA
ENST00000293778.10:c.*470_*471insA ENSP00000293778.6:n.*470_*471insA
ENST00000576153.5:n.1026_1027insA
NM_022059.3:c.*470_*471insA NP_071342.2:n.*470_*471insA
NM_022059.4:c.*470_*471insA NP_071342.2:n.*470_*471insA
NM_001386809.1:c.*470_*471insA MANE Select NP_001373738.1:n.*470_*471insA
Search 100 bp 5'
Search 100 bp 3'