Canonical Allele Identifier: CA2237486688
Gene: HSD17B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82095753A= , CM000678.2:g.82095753A= GRCh38
NC_000016.9:g.82129358A= , CM000678.1:g.82129358A= GRCh37
NC_000016.8:g.80686859A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000199936.9:c.803-2322A= MANE Select ENSP00000199936.4:n.803-2322A=
ENST00000199936.8:c.803-2322A= ENSP00000199936.4:n.803-2322A=
ENST00000566838.2:c.5144A= ENSP00000456471.1:n.5144A=
ENST00000568090.5:c.395-2322A= ENSP00000456529.1:n.395-2322A=
NM_002153.2:c.803-2322A= NP_002144.1:n.803-2322A=
XR_001751898.2:n.1021-2322A=
NM_002153.3:c.803-2322A= MANE Select NP_002144.1:n.803-2322A=