Canonical Allele Identifier: CA466132244

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.99006656G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96244374G>T , CM000671.2:g.96244374G>T	GRCh38
NC_000009.11:g.99006656G>T , CM000671.1:g.99006656G>T	GRCh37
NC_000009.10:g.98046477G>T	NCBI36
NG_008157.1:g.62779C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.627C>A	ENSP00000364411.2:p.Ser209=
ENST00000375263.8:c.627C>A MANE Select	ENSP00000364412.3:p.Ser209=
ENST00000463517.2:n.2169C>A
ENST00000464104.6:n.1565C>A
ENST00000467499.6:c.*326C>A	ENSP00000498077.1:n.*326C>A
ENST00000494814.6:n.139C>A
ENST00000643789.1:c.2919C>A
ENST00000648146.1:c.627C>A	ENSP00000497238.1:p.Ser209=
ENST00000648332.1:c.304C>A	ENSP00000497562.1:p.Gln102Lys
ENST00000648799.1:c.519C>A	ENSP00000498039.1:p.Ser173=
ENST00000650005.1:c.556C>A	ENSP00000498121.1:p.Gln186Lys
ENST00000375262.3:c.627C>A	ENSP00000364411.2:p.Ser209=
ENST00000375263.7:c.627C>A	ENSP00000364412.3:p.Ser209=
ENST00000464104.5:n.480C>A
ENST00000494814.5:n.148C>A
NM_000197.1:c.627C>A	NP_000188.1:p.Ser209=
XM_005251970.3:c.267C>A	XP_005252027.1:p.Ser89=
XM_011518618.1:c.627C>A	XP_011516920.1:p.Ser209=
XM_011518619.1:c.627C>A	XP_011516921.1:p.Ser209=
XM_011518620.1:c.519C>A	XP_011516922.1:p.Ser173=
XM_011518621.1:c.627C>A	XP_011516923.1:p.Ser209=
NM_000197.2:c.627C>A MANE Select	NP_000188.1:p.Ser209=
XM_011518618.2:c.627C>A	XP_011516920.1:p.Ser209=
XM_011518619.2:c.627C>A	XP_011516921.1:p.Ser209=
XM_017014671.1:c.627C>A	XP_016870160.1:p.Ser209=
XM_017014672.1:c.627C>A	XP_016870161.1:p.Ser209=
XM_017014673.2:c.591C>A	XP_016870162.1:p.Ser197=
XM_017014674.1:c.519C>A	XP_016870163.1:p.Ser173=
XM_017014675.1:c.465C>A	XP_016870164.1:p.Ser155=
XM_017014677.1:c.267C>A	XP_016870166.1:p.Ser89=
XM_024447529.1:c.465C>A	XP_024303297.1:p.Ser155=
XR_002956778.1:n.3061C>A