Canonical Allele Identifier: CA2807857793
Gene: HSD17B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82095567T>A , CM000678.2:g.82095567T>A GRCh38
NC_000016.9:g.82129172T>A , CM000678.1:g.82129172T>A GRCh37
NC_000016.8:g.80686673T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000199936.9:c.803-2508T>A MANE Select ENSP00000199936.4:n.803-2508T>A
ENST00000199936.8:c.803-2508T>A ENSP00000199936.4:n.803-2508T>A
ENST00000566838.2:c.4958T>A ENSP00000456471.1:n.4958T>A
ENST00000568090.5:c.395-2508T>A ENSP00000456529.1:n.395-2508T>A
NM_002153.2:c.803-2508T>A NP_002144.1:n.803-2508T>A
XR_001751898.2:n.1021-2508T>A
NM_002153.3:c.803-2508T>A MANE Select NP_002144.1:n.803-2508T>A
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