Canonical Allele Identifier: CA466129704

Gene: HSD17B3

Linked Data

• dbSNP Id: rs1587704518
• MyVariant Identifiers: chr9:g.98997832G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235550G>A , CM000671.2:g.96235550G>A	GRCh38
NC_000009.11:g.98997832G>A , CM000671.1:g.98997832G>A	GRCh37
NC_000009.10:g.98037653G>A	NCBI36
NG_008157.1:g.71603C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375262.4:c.693C>T	ENSP00000364411.2:p.Ile231=
ENST00000375263.8:c.843C>T MANE Select	ENSP00000364412.3:p.Ile281=
ENST00000463517.2:n.2385C>T
ENST00000464104.6:n.1781C>T
ENST00000467499.6:c.*542C>T	ENSP00000498077.1:n.*542C>T
ENST00000494814.6:n.393C>T
ENST00000643789.1:c.3135C>T
ENST00000648146.1:c.981C>T	ENSP00000497238.1:n.981C>T
ENST00000648332.1:c.520C>T	ENSP00000497562.1:n.520C>T
ENST00000648799.1:c.735C>T	ENSP00000498039.1:p.Ile245=
ENST00000650005.1:c.772C>T	ENSP00000498121.1:n.772C>T
ENST00000375262.3:c.693C>T	ENSP00000364411.2:p.Ile231=
ENST00000375263.7:c.843C>T	ENSP00000364412.3:p.Ile281=
ENST00000464104.5:n.696C>T
ENST00000467499.5:n.103C>T
ENST00000494814.5:n.402C>T
NM_000197.1:c.843C>T	NP_000188.1:p.Ile281=
XM_005251970.3:c.483C>T	XP_005252027.1:p.Ile161=
XM_011518618.1:c.843C>T	XP_011516920.1:p.Ile281=
XM_011518619.1:c.843C>T	XP_011516921.1:p.Ile281=
XM_011518620.1:c.735C>T	XP_011516922.1:p.Ile245=
NM_000197.2:c.843C>T MANE Select	NP_000188.1:p.Ile281=
XM_011518618.2:c.843C>T	XP_011516920.1:p.Ile281=
XM_011518619.2:c.843C>T	XP_011516921.1:p.Ile281=
XM_017014671.1:c.843C>T	XP_016870160.1:p.Ile281=
XM_017014672.1:c.843C>T	XP_016870161.1:p.Ile281=
XM_017014673.2:c.807C>T	XP_016870162.1:p.Ile269=
XM_017014674.1:c.735C>T	XP_016870163.1:p.Ile245=
XM_017014675.1:c.681C>T	XP_016870164.1:p.Ile227=
XM_017014677.1:c.483C>T	XP_016870166.1:p.Ile161=
XM_024447529.1:c.681C>T	XP_024303297.1:p.Ile227=
XR_002956778.1:n.3315C>T