Canonical Allele Identifier: CA1865988516

Gene: HSD17B3

Linked Data

• dbSNP Id: rs1587717258

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96244872G>T , CM000671.2:g.96244872G>T	GRCh38
NC_000009.11:g.99007154G>T , CM000671.1:g.99007154G>T	GRCh37
NC_000009.10:g.98046975G>T	NCBI36
NG_008157.1:g.62281C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375262.4:c.606+473C>A	ENSP00000364411.2:n.606+473C>A
ENST00000375263.8:c.606+473C>A MANE Select	ENSP00000364412.3:n.606+473C>A
ENST00000463517.2:n.2127-456C>A
ENST00000464104.6:n.1544+473C>A
ENST00000467499.6:c.*305+473C>A	ENSP00000498077.1:n.*305+473C>A
ENST00000494814.6:n.118+473C>A
ENST00000643789.1:c.2898+473C>A
ENST00000648146.1:c.606+473C>A	ENSP00000497238.1:n.606+473C>A
ENST00000648332.1:c.283+473C>A	ENSP00000497562.1:n.283+473C>A
ENST00000648799.1:c.498+473C>A	ENSP00000498039.1:n.498+473C>A
ENST00000650005.1:c.535+473C>A	ENSP00000498121.1:n.535+473C>A
ENST00000375262.3:c.606+473C>A	ENSP00000364411.2:n.606+473C>A
ENST00000375263.7:c.606+473C>A	ENSP00000364412.3:n.606+473C>A
ENST00000464104.5:n.459+473C>A
ENST00000494814.5:n.127+473C>A
NM_000197.1:c.606+473C>A	NP_000188.1:n.606+473C>A
XM_005251970.3:c.246+473C>A	XP_005252027.1:n.246+473C>A
XM_011518618.1:c.606+473C>A	XP_011516920.1:n.606+473C>A
XM_011518619.1:c.606+473C>A	XP_011516921.1:n.606+473C>A
XM_011518620.1:c.498+473C>A	XP_011516922.1:n.498+473C>A
XM_011518621.1:c.606+473C>A	XP_011516923.1:n.606+473C>A
NM_000197.2:c.606+473C>A MANE Select	NP_000188.1:n.606+473C>A
XM_011518618.2:c.606+473C>A	XP_011516920.1:n.606+473C>A
XM_011518619.2:c.606+473C>A	XP_011516921.1:n.606+473C>A
XM_017014671.1:c.606+473C>A	XP_016870160.1:n.606+473C>A
XM_017014672.1:c.606+473C>A	XP_016870161.1:n.606+473C>A
XM_017014673.2:c.570+473C>A	XP_016870162.1:n.570+473C>A
XM_017014674.1:c.498+473C>A	XP_016870163.1:n.498+473C>A
XM_017014675.1:c.444+473C>A	XP_016870164.1:n.444+473C>A
XM_017014677.1:c.246+473C>A	XP_016870166.1:n.246+473C>A
XM_024447529.1:c.444+473C>A	XP_024303297.1:n.444+473C>A
XR_002956778.1:n.3040+473C>A