Canonical Allele Identifier: CA466129811

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.98998114G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235832G>C , CM000671.2:g.96235832G>C	GRCh38
NC_000009.11:g.98998114G>C , CM000671.1:g.98998114G>C	GRCh37
NC_000009.10:g.98037935G>C	NCBI36
NG_008157.1:g.71321C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.673-262C>G	ENSP00000364411.2:n.673-262C>G
ENST00000375263.8:c.823-262C>G MANE Select	ENSP00000364412.3:n.823-262C>G
ENST00000463517.2:n.2365-262C>G
ENST00000464104.6:n.1761-262C>G
ENST00000467499.6:c.*522-262C>G	ENSP00000498077.1:n.*522-262C>G
ENST00000494814.6:n.373-262C>G
ENST00000643789.1:c.3115-262C>G
ENST00000648146.1:c.961-262C>G	ENSP00000497238.1:n.961-262C>G
ENST00000648332.1:c.500-262C>G	ENSP00000497562.1:n.500-262C>G
ENST00000648799.1:c.715-262C>G	ENSP00000498039.1:n.715-262C>G
ENST00000650005.1:c.752-262C>G	ENSP00000498121.1:n.752-262C>G
ENST00000375262.3:c.673-262C>G	ENSP00000364411.2:n.673-262C>G
ENST00000375263.7:c.823-262C>G	ENSP00000364412.3:n.823-262C>G
ENST00000464104.5:n.676-262C>G
ENST00000467499.5:n.83-262C>G
ENST00000494814.5:n.382-262C>G
NM_000197.1:c.823-262C>G	NP_000188.1:n.823-262C>G
XM_005251970.3:c.463-262C>G	XP_005252027.1:n.463-262C>G
XM_011518618.1:c.823-262C>G	XP_011516920.1:n.823-262C>G
XM_011518619.1:c.823-262C>G	XP_011516921.1:n.823-262C>G
XM_011518620.1:c.715-262C>G	XP_011516922.1:n.715-262C>G
NM_000197.2:c.823-262C>G MANE Select	NP_000188.1:n.823-262C>G
XM_011518618.2:c.823-262C>G	XP_011516920.1:n.823-262C>G
XM_011518619.2:c.823-262C>G	XP_011516921.1:n.823-262C>G
XM_017014671.1:c.823-262C>G	XP_016870160.1:n.823-262C>G
XM_017014672.1:c.823-262C>G	XP_016870161.1:n.823-262C>G
XM_017014673.2:c.787-262C>G	XP_016870162.1:n.787-262C>G
XM_017014674.1:c.715-262C>G	XP_016870163.1:n.715-262C>G
XM_017014675.1:c.661-262C>G	XP_016870164.1:n.661-262C>G
XM_017014677.1:c.463-262C>G	XP_016870166.1:n.463-262C>G
XM_024447529.1:c.661-262C>G	XP_024303297.1:n.661-262C>G
XR_002956778.1:n.3295-262C>G