Canonical Allele Identifier: CA2237486789
Gene: HSD17B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82095816C= , CM000678.2:g.82095816C= GRCh38
NC_000016.9:g.82129421C= , CM000678.1:g.82129421C= GRCh37
NC_000016.8:g.80686922C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000199936.9:c.803-2259C= MANE Select ENSP00000199936.4:n.803-2259C=
ENST00000199936.8:c.803-2259C= ENSP00000199936.4:n.803-2259C=
ENST00000566838.2:c.5207C= ENSP00000456471.1:n.5207C=
ENST00000568090.5:c.395-2259C= ENSP00000456529.1:n.395-2259C=
NM_002153.2:c.803-2259C= NP_002144.1:n.803-2259C=
XR_001751898.2:n.1021-2259C=
NM_002153.3:c.803-2259C= MANE Select NP_002144.1:n.803-2259C=