Canonical Allele Identifier: CA374126438

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.99060744A>C (hg19) ; chr9:g.96298462A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96298462A>C , CM000671.2:g.96298462A>C	GRCh38
NC_000009.11:g.99060744A>C , CM000671.1:g.99060744A>C	GRCh37
NC_000009.10:g.98100565A>C	NCBI36
NG_008157.1:g.8691T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.155T>G	ENSP00000364411.2:p.Val52Gly
ENST00000375263.8:c.155T>G MANE Select	ENSP00000364412.3:p.Val52Gly
ENST00000463517.2:n.964T>G
ENST00000464104.6:n.625T>G
ENST00000467499.6:c.155T>G	ENSP00000498077.1:p.Val52Gly
ENST00000643789.1:c.2447T>G
ENST00000648146.1:c.155T>G	ENSP00000497238.1:p.Val52Gly
ENST00000648332.1:c.155T>G	ENSP00000497562.1:p.Val52Gly
ENST00000648799.1:c.155T>G	ENSP00000498039.1:p.Val52Gly
ENST00000650005.1:c.155T>G	ENSP00000498121.1:p.Val52Gly
ENST00000650386.1:c.155T>G	ENSP00000497464.1:p.Val52Gly
ENST00000375262.3:c.155T>G	ENSP00000364411.2:p.Val52Gly
ENST00000375263.7:c.155T>G	ENSP00000364412.3:p.Val52Gly
NM_000197.1:c.155T>G	NP_000188.1:p.Val52Gly
XM_006717095.2:c.155T>G	XP_006717158.1:p.Val52Gly
XM_011518618.1:c.155T>G	XP_011516920.1:p.Val52Gly
XM_011518619.1:c.155T>G	XP_011516921.1:p.Val52Gly
XM_011518620.1:c.155T>G	XP_011516922.1:p.Val52Gly
XM_011518621.1:c.155T>G	XP_011516923.1:p.Val52Gly
NM_000197.2:c.155T>G MANE Select	NP_000188.1:p.Val52Gly
XM_011518618.2:c.155T>G	XP_011516920.1:p.Val52Gly
XM_011518619.2:c.155T>G	XP_011516921.1:p.Val52Gly
XM_017014671.1:c.155T>G	XP_016870160.1:p.Val52Gly
XM_017014672.1:c.155T>G	XP_016870161.1:p.Val52Gly
XM_017014673.2:c.155T>G	XP_016870162.1:p.Val52Gly
XM_017014674.1:c.155T>G	XP_016870163.1:p.Val52Gly
XM_017014675.1:c.69T>G	XP_016870164.1:p.Ser23Arg
XM_017014677.1:c.-782T>G	XP_016870166.1:n.-782T>G
XM_024447529.1:c.69T>G	XP_024303297.1:p.Ser23Arg
XR_002956778.1:n.2589T>G