Canonical Allele Identifier: CA1865989914

Gene: HSD17B3 HSD17B3-AS1

Linked Data

• dbSNP Id: rs1836649935

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96246064G>A , CM000671.2:g.96246064G>A	GRCh38
NC_000009.11:g.99008346G>A , CM000671.1:g.99008346G>A	GRCh37
NC_000009.10:g.98048167G>A	NCBI36
NG_008157.1:g.61089C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375262.4:c.524+492C>T (HSD17B3)	ENSP00000364411.2:n.524+492C>T
ENST00000375263.8:c.524+492C>T (HSD17B3) MANE Select	ENSP00000364412.3:n.524+492C>T
ENST00000463517.2:n.2044+492C>T
ENST00000464104.6:n.1462+492C>T
ENST00000467499.6:c.*223+492C>T (HSD17B3)	ENSP00000498077.1:n.*223+492C>T
ENST00000494814.6:n.37-638C>T (HSD17B3)
ENST00000643789.1:c.2816+492C>T
ENST00000648146.1:c.524+492C>T (HSD17B3)	ENSP00000497238.1:n.524+492C>T
ENST00000648332.1:c.202-638C>T (HSD17B3)	ENSP00000497562.1:n.202-638C>T
ENST00000648799.1:c.416+492C>T (HSD17B3)	ENSP00000498039.1:n.416+492C>T
ENST00000650005.1:c.454-638C>T (HSD17B3)	ENSP00000498121.1:n.454-638C>T
ENST00000375262.3:c.524+492C>T (HSD17B3)	ENSP00000364411.2:n.524+492C>T
ENST00000375263.7:c.524+492C>T (HSD17B3)	ENSP00000364412.3:n.524+492C>T
ENST00000464104.5:n.377+492C>T (HSD17B3)
ENST00000494814.5:n.46-638C>T (HSD17B3)
NM_000197.1:c.524+492C>T (HSD17B3)	NP_000188.1:n.524+492C>T
XM_005251970.3:c.164+492C>T (HSD17B3)	XP_005252027.1:n.164+492C>T
XM_011518618.1:c.524+492C>T (HSD17B3)	XP_011516920.1:n.524+492C>T
XM_011518619.1:c.524+492C>T (HSD17B3)	XP_011516921.1:n.524+492C>T
XM_011518620.1:c.416+492C>T (HSD17B3)	XP_011516922.1:n.416+492C>T
XM_011518621.1:c.524+492C>T (HSD17B3)	XP_011516923.1:n.524+492C>T
XR_930147.1:n.630G>A (HSD17B3-AS1)
XR_930148.1:n.630G>A (HSD17B3-AS1)
NM_000197.2:c.524+492C>T (HSD17B3) MANE Select	NP_000188.1:n.524+492C>T
XM_011518618.2:c.524+492C>T (HSD17B3)	XP_011516920.1:n.524+492C>T
XM_011518619.2:c.524+492C>T (HSD17B3)	XP_011516921.1:n.524+492C>T
XM_017014671.1:c.524+492C>T (HSD17B3)	XP_016870160.1:n.524+492C>T
XM_017014672.1:c.524+492C>T (HSD17B3)	XP_016870161.1:n.524+492C>T
XM_017014673.2:c.488+492C>T (HSD17B3)	XP_016870162.1:n.488+492C>T
XM_017014674.1:c.416+492C>T (HSD17B3)	XP_016870163.1:n.416+492C>T
XM_017014675.1:c.362+492C>T (HSD17B3)	XP_016870164.1:n.362+492C>T
XM_017014677.1:c.164+492C>T (HSD17B3)	XP_016870166.1:n.164+492C>T
XM_024447529.1:c.362+492C>T (HSD17B3)	XP_024303297.1:n.362+492C>T
XR_002956778.1:n.2958+492C>T (HSD17B3)