Canonical Allele Identifier: CA374121814

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.98997801G>C (hg19) ; chr9:g.96235519G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235519G>C , CM000671.2:g.96235519G>C	GRCh38
NC_000009.11:g.98997801G>C , CM000671.1:g.98997801G>C	GRCh37
NC_000009.10:g.98037622G>C	NCBI36
NG_008157.1:g.71634C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.724C>G	ENSP00000364411.2:p.Gln242Glu
ENST00000375263.8:c.874C>G MANE Select	ENSP00000364412.3:p.Gln292Glu
ENST00000463517.2:n.2416C>G
ENST00000464104.6:n.1812C>G
ENST00000467499.6:c.*573C>G	ENSP00000498077.1:n.*573C>G
ENST00000494814.6:n.424C>G
ENST00000643789.1:c.3166C>G
ENST00000648146.1:c.1012C>G	ENSP00000497238.1:n.1012C>G
ENST00000648332.1:c.551C>G	ENSP00000497562.1:n.551C>G
ENST00000650005.1:c.803C>G	ENSP00000498121.1:n.803C>G
ENST00000375262.3:c.724C>G	ENSP00000364411.2:p.Gln242Glu
ENST00000375263.7:c.874C>G	ENSP00000364412.3:p.Gln292Glu
ENST00000464104.5:n.727C>G
ENST00000467499.5:n.134C>G
ENST00000494814.5:n.433C>G
NM_000197.1:c.874C>G	NP_000188.1:p.Gln292Glu
XM_005251970.3:c.514C>G	XP_005252027.1:p.Gln172Glu
XM_011518618.1:c.874C>G	XP_011516920.1:p.Gln292Glu
XM_011518619.1:c.874C>G	XP_011516921.1:p.Gln292Glu
XM_011518620.1:c.766C>G	XP_011516922.1:p.Gln256Glu
NM_000197.2:c.874C>G MANE Select	NP_000188.1:p.Gln292Glu
XM_011518618.2:c.874C>G	XP_011516920.1:p.Gln292Glu
XM_011518619.2:c.874C>G	XP_011516921.1:p.Gln292Glu
XM_017014671.1:c.874C>G	XP_016870160.1:p.Gln292Glu
XM_017014672.1:c.874C>G	XP_016870161.1:p.Gln292Glu
XM_017014673.2:c.838C>G	XP_016870162.1:p.Gln280Glu
XM_017014674.1:c.766C>G	XP_016870163.1:p.Gln256Glu
XM_017014675.1:c.712C>G	XP_016870164.1:p.Gln238Glu
XM_017014677.1:c.514C>G	XP_016870166.1:p.Gln172Glu
XM_024447529.1:c.712C>G	XP_024303297.1:p.Gln238Glu
XR_002956778.1:n.3346C>G