Canonical Allele Identifier: CA2038557421
Gene: HSD17B6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56769532C>A , CM000674.2:g.56769532C>A GRCh38
NC_000012.11:g.57163316C>A , CM000674.1:g.57163316C>A GRCh37
NC_000012.10:g.55449583C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000322165.1:c.-19-4302C>A MANE Select ENSP00000318631.1:n.-19-4302C>A
ENST00000554150.5:c.-19-4302C>A ENSP00000452273.1:n.-19-4302C>A
ENST00000554155.1:c.-14-4307C>A ENSP00000451497.1:n.-14-4307C>A
ENST00000554643.5:c.-19-4302C>A ENSP00000451406.1:n.-19-4302C>A
ENST00000555159.5:c.-19-4302C>A ENSP00000450698.1:n.-19-4302C>A
ENST00000555805.5:c.-19-4302C>A ENSP00000451753.1:n.-19-4302C>A
ENST00000556481.5:n.343-783C>A
ENST00000556650.5:c.-19-4302C>A ENSP00000452103.1:n.-19-4302C>A
NM_003725.3:c.-19-4302C>A NP_003716.2:n.-19-4302C>A
XM_005269207.1:c.-19-4302C>A XP_005269264.1:n.-19-4302C>A
XM_005269208.1:c.-19-4302C>A XP_005269265.1:n.-19-4302C>A
XM_005269209.1:c.-14-4307C>A XP_005269266.1:n.-14-4307C>A
XM_006719672.1:c.-14-4307C>A XP_006719735.1:n.-14-4307C>A
XM_011538925.1:c.-19-4302C>A XP_011537227.1:n.-19-4302C>A
XM_011538926.1:c.-19-4302C>A XP_011537228.1:n.-19-4302C>A
XM_011538927.1:c.-14-4307C>A XP_011537229.1:n.-14-4307C>A
XR_245961.1:n.347-4302C>A
XM_024449249.1:c.-19-4302C>A XP_024305017.1:n.-19-4302C>A
XM_024449250.1:c.-19-4302C>A XP_024305018.1:n.-19-4302C>A
XM_024449251.1:c.-19-4302C>A XP_024305019.1:n.-19-4302C>A
NM_003725.4:c.-19-4302C>A MANE Select NP_003716.2:n.-19-4302C>A