Canonical Allele Identifier: CA2237486468
Gene: HSD17B2 HGNC NCBI

Linked Data

dbSNP Id: rs1904817095
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82095586del , CM000678.2:g.82095586del GRCh38
NC_000016.9:g.82129191del , CM000678.1:g.82129191del GRCh37
NC_000016.8:g.80686692del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000199936.9:c.803-2489del MANE Select ENSP00000199936.4:n.803-2489del
ENST00000199936.8:c.803-2489del ENSP00000199936.4:n.803-2489del
ENST00000566838.2:c.4977del ENSP00000456471.1:n.4977del
ENST00000568090.5:c.395-2489del ENSP00000456529.1:n.395-2489del
NM_002153.2:c.803-2489del NP_002144.1:n.803-2489del
XR_001751898.2:n.1021-2489del
NM_002153.3:c.803-2489del MANE Select NP_002144.1:n.803-2489del
Search 100 bp 5'
Search 100 bp 3'