Canonical Allele Identifier: CA2807857798

Gene: HSD17B2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.82095789C>T , CM000678.2:g.82095789C>T	GRCh38
NC_000016.9:g.82129394C>T , CM000678.1:g.82129394C>T	GRCh37
NC_000016.8:g.80686895C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000199936.9:c.803-2286C>T MANE Select	ENSP00000199936.4:n.803-2286C>T
ENST00000199936.8:c.803-2286C>T	ENSP00000199936.4:n.803-2286C>T
ENST00000566838.2:c.5180C>T	ENSP00000456471.1:n.5180C>T
ENST00000568090.5:c.395-2286C>T	ENSP00000456529.1:n.395-2286C>T
NM_002153.2:c.803-2286C>T	NP_002144.1:n.803-2286C>T
XR_001751898.2:n.1021-2286C>T
NM_002153.3:c.803-2286C>T MANE Select	NP_002144.1:n.803-2286C>T