Canonical Allele Identifier: CA2237486455
Gene: HSD17B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82095582C= , CM000678.2:g.82095582C= GRCh38
NC_000016.9:g.82129187C= , CM000678.1:g.82129187C= GRCh37
NC_000016.8:g.80686688C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000199936.9:c.803-2493C= MANE Select ENSP00000199936.4:n.803-2493C=
ENST00000199936.8:c.803-2493C= ENSP00000199936.4:n.803-2493C=
ENST00000566838.2:c.4973C= ENSP00000456471.1:n.4973C=
ENST00000568090.5:c.395-2493C= ENSP00000456529.1:n.395-2493C=
NM_002153.2:c.803-2493C= NP_002144.1:n.803-2493C=
XR_001751898.2:n.1021-2493C=
NM_002153.3:c.803-2493C= MANE Select NP_002144.1:n.803-2493C=
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