Canonical Allele Identifier: CA466129647

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.98997808A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235526A>G , CM000671.2:g.96235526A>G	GRCh38
NC_000009.11:g.98997808A>G , CM000671.1:g.98997808A>G	GRCh37
NC_000009.10:g.98037629A>G	NCBI36
NG_008157.1:g.71627T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.717T>C	ENSP00000364411.2:p.Gly239=
ENST00000375263.8:c.867T>C MANE Select	ENSP00000364412.3:p.Gly289=
ENST00000463517.2:n.2409T>C
ENST00000464104.6:n.1805T>C
ENST00000467499.6:c.*566T>C	ENSP00000498077.1:n.*566T>C
ENST00000494814.6:n.417T>C
ENST00000643789.1:c.3159T>C
ENST00000648146.1:c.1005T>C	ENSP00000497238.1:n.1005T>C
ENST00000648332.1:c.544T>C	ENSP00000497562.1:n.544T>C
ENST00000650005.1:c.796T>C	ENSP00000498121.1:n.796T>C
ENST00000375262.3:c.717T>C	ENSP00000364411.2:p.Gly239=
ENST00000375263.7:c.867T>C	ENSP00000364412.3:p.Gly289=
ENST00000464104.5:n.720T>C
ENST00000467499.5:n.127T>C
ENST00000494814.5:n.426T>C
NM_000197.1:c.867T>C	NP_000188.1:p.Gly289=
XM_005251970.3:c.507T>C	XP_005252027.1:p.Gly169=
XM_011518618.1:c.867T>C	XP_011516920.1:p.Gly289=
XM_011518619.1:c.867T>C	XP_011516921.1:p.Gly289=
XM_011518620.1:c.759T>C	XP_011516922.1:p.Gly253=
NM_000197.2:c.867T>C MANE Select	NP_000188.1:p.Gly289=
XM_011518618.2:c.867T>C	XP_011516920.1:p.Gly289=
XM_011518619.2:c.867T>C	XP_011516921.1:p.Gly289=
XM_017014671.1:c.867T>C	XP_016870160.1:p.Gly289=
XM_017014672.1:c.867T>C	XP_016870161.1:p.Gly289=
XM_017014673.2:c.831T>C	XP_016870162.1:p.Gly277=
XM_017014674.1:c.759T>C	XP_016870163.1:p.Gly253=
XM_017014675.1:c.705T>C	XP_016870164.1:p.Gly235=
XM_017014677.1:c.507T>C	XP_016870166.1:p.Gly169=
XM_024447529.1:c.705T>C	XP_024303297.1:p.Gly235=
XR_002956778.1:n.3339T>C