Canonical Allele Identifier: CA2720354198

Gene: HSD17B3

Linked Data

• dbSNP Id: rs2130799664

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96298200dup , CM000671.2:g.96298200dup	GRCh38
NC_000009.11:g.99060482dup , CM000671.1:g.99060482dup	GRCh37
NC_000009.10:g.98100303dup	NCBI36
NG_008157.1:g.8954dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.201+217dup	ENSP00000364411.2:n.201+217dup
ENST00000375263.8:c.201+217dup MANE Select	ENSP00000364412.3:n.201+217dup
ENST00000463517.2:n.1010+217dup
ENST00000464104.6:n.671+217dup
ENST00000467499.6:c.201+217dup	ENSP00000498077.1:n.201+217dup
ENST00000643789.1:c.2493+217dup
ENST00000648146.1:c.201+217dup	ENSP00000497238.1:n.201+217dup
ENST00000648332.1:c.201+217dup	ENSP00000497562.1:n.201+217dup
ENST00000648799.1:c.201+217dup	ENSP00000498039.1:n.201+217dup
ENST00000650005.1:c.201+217dup	ENSP00000498121.1:n.201+217dup
ENST00000650386.1:c.201+217dup	ENSP00000497464.1:n.201+217dup
ENST00000375262.3:c.201+217dup	ENSP00000364411.2:n.201+217dup
ENST00000375263.7:c.201+217dup	ENSP00000364412.3:n.201+217dup
NM_000197.1:c.201+217dup	NP_000188.1:n.201+217dup
XM_006717095.2:c.201+217dup	XP_006717158.1:n.201+217dup
XM_011518618.1:c.201+217dup	XP_011516920.1:n.201+217dup
XM_011518619.1:c.201+217dup	XP_011516921.1:n.201+217dup
XM_011518620.1:c.201+217dup	XP_011516922.1:n.201+217dup
XM_011518621.1:c.201+217dup	XP_011516923.1:n.201+217dup
NM_000197.2:c.201+217dup MANE Select	NP_000188.1:n.201+217dup
XM_011518618.2:c.201+217dup	XP_011516920.1:n.201+217dup
XM_011518619.2:c.201+217dup	XP_011516921.1:n.201+217dup
XM_017014671.1:c.201+217dup	XP_016870160.1:n.201+217dup
XM_017014672.1:c.201+217dup	XP_016870161.1:n.201+217dup
XM_017014673.2:c.201+217dup	XP_016870162.1:n.201+217dup
XM_017014674.1:c.201+217dup	XP_016870163.1:n.201+217dup
XM_017014675.1:c.115+217dup	XP_016870164.1:n.115+217dup
XM_017014677.1:c.-736+217dup	XP_016870166.1:n.-736+217dup
XM_024447529.1:c.115+217dup	XP_024303297.1:n.115+217dup
XR_002956778.1:n.2635+217dup