Canonical Allele Identifier: CA2634536782
Gene: HSD17B2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82095756del , CM000678.2:g.82095756del GRCh38
NC_000016.9:g.82129361del , CM000678.1:g.82129361del GRCh37
NC_000016.8:g.80686862del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000199936.9:c.803-2319del MANE Select ENSP00000199936.4:n.803-2319del
ENST00000199936.8:c.803-2319del ENSP00000199936.4:n.803-2319del
ENST00000566838.2:c.5147del ENSP00000456471.1:n.5147del
ENST00000568090.5:c.395-2319del ENSP00000456529.1:n.395-2319del
NM_002153.2:c.803-2319del NP_002144.1:n.803-2319del
XR_001751898.2:n.1021-2319del
NM_002153.3:c.803-2319del MANE Select NP_002144.1:n.803-2319del