Canonical Allele Identifier: CA374121536

Gene: HSD17B3

Linked Data

• MyVariant Identifiers: chr9:g.98997749A>G (hg19) ; chr9:g.96235467A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96235467A>G , CM000671.2:g.96235467A>G	GRCh38
NC_000009.11:g.98997749A>G , CM000671.1:g.98997749A>G	GRCh37
NC_000009.10:g.98037570A>G	NCBI36
NG_008157.1:g.71686T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.776T>C	ENSP00000364411.2:p.Val259Ala
ENST00000375263.8:c.926T>C MANE Select	ENSP00000364412.3:p.Val309Ala
ENST00000463517.2:n.2468T>C
ENST00000464104.6:n.1864T>C
ENST00000467499.6:c.*625T>C	ENSP00000498077.1:n.*625T>C
ENST00000494814.6:n.476T>C
ENST00000643789.1:c.3218T>C
ENST00000648146.1:c.1064T>C	ENSP00000497238.1:n.1064T>C
ENST00000648332.1:c.603T>C	ENSP00000497562.1:n.603T>C
ENST00000650005.1:c.855T>C	ENSP00000498121.1:n.855T>C
ENST00000375262.3:c.776T>C	ENSP00000364411.2:p.Val259Ala
ENST00000375263.7:c.926T>C	ENSP00000364412.3:p.Val309Ala
ENST00000464104.5:n.779T>C
ENST00000467499.5:n.186T>C
ENST00000494814.5:n.485T>C
NM_000197.1:c.926T>C	NP_000188.1:p.Val309Ala
XM_005251970.3:c.566T>C	XP_005252027.1:p.Val189Ala
XM_011518618.1:c.926T>C	XP_011516920.1:p.Val309Ala
XM_011518619.1:c.926T>C	XP_011516921.1:p.Val309Ala
XM_011518620.1:c.818T>C	XP_011516922.1:p.Val273Ala
NM_000197.2:c.926T>C MANE Select	NP_000188.1:p.Val309Ala
XM_011518618.2:c.926T>C	XP_011516920.1:p.Val309Ala
XM_011518619.2:c.926T>C	XP_011516921.1:p.Val309Ala
XM_017014671.1:c.926T>C	XP_016870160.1:p.Val309Ala
XM_017014672.1:c.926T>C	XP_016870161.1:p.Val309Ala
XM_017014673.2:c.890T>C	XP_016870162.1:p.Val297Ala
XM_017014674.1:c.818T>C	XP_016870163.1:p.Val273Ala
XM_017014675.1:c.764T>C	XP_016870164.1:p.Val255Ala
XM_017014677.1:c.566T>C	XP_016870166.1:p.Val189Ala
XM_024447529.1:c.764T>C	XP_024303297.1:p.Val255Ala
XR_002956778.1:n.3398T>C