Canonical Allele Identifier: CA1865990057
Gene: HSD17B3 HGNC NCBI
HSD17B3-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2253502

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.96246161G>C , CM000671.2:g.96246161G>C GRCh38
NC_000009.11:g.99008443G>C , CM000671.1:g.99008443G>C GRCh37
NC_000009.10:g.98048264G>C NCBI36
NG_008157.1:g.60992C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375262.4:c.524+395C>G (HSD17B3) ENSP00000364411.2:n.524+395C>G
ENST00000375263.8:c.524+395C>G (HSD17B3) MANE Select ENSP00000364412.3:n.524+395C>G
ENST00000463517.2:n.2044+395C>G
ENST00000464104.6:n.1462+395C>G
ENST00000467499.6:c.*223+395C>G (HSD17B3) ENSP00000498077.1:n.*223+395C>G
ENST00000494814.6:n.37-735C>G (HSD17B3)
ENST00000643789.1:c.2816+395C>G
ENST00000648146.1:c.524+395C>G (HSD17B3) ENSP00000497238.1:n.524+395C>G
ENST00000648332.1:c.202-735C>G (HSD17B3) ENSP00000497562.1:n.202-735C>G
ENST00000648799.1:c.416+395C>G (HSD17B3) ENSP00000498039.1:n.416+395C>G
ENST00000650005.1:c.454-735C>G (HSD17B3) ENSP00000498121.1:n.454-735C>G
ENST00000375262.3:c.524+395C>G (HSD17B3) ENSP00000364411.2:n.524+395C>G
ENST00000375263.7:c.524+395C>G (HSD17B3) ENSP00000364412.3:n.524+395C>G
ENST00000464104.5:n.377+395C>G (HSD17B3)
ENST00000494814.5:n.46-735C>G (HSD17B3)
NM_000197.1:c.524+395C>G (HSD17B3) NP_000188.1:n.524+395C>G
XM_005251970.3:c.164+395C>G (HSD17B3) XP_005252027.1:n.164+395C>G
XM_011518618.1:c.524+395C>G (HSD17B3) XP_011516920.1:n.524+395C>G
XM_011518619.1:c.524+395C>G (HSD17B3) XP_011516921.1:n.524+395C>G
XM_011518620.1:c.416+395C>G (HSD17B3) XP_011516922.1:n.416+395C>G
XM_011518621.1:c.524+395C>G (HSD17B3) XP_011516923.1:n.524+395C>G
XR_930147.1:n.727G>C (HSD17B3-AS1)
XR_930148.1:n.727G>C (HSD17B3-AS1)
NM_000197.2:c.524+395C>G (HSD17B3) MANE Select NP_000188.1:n.524+395C>G
XM_011518618.2:c.524+395C>G (HSD17B3) XP_011516920.1:n.524+395C>G
XM_011518619.2:c.524+395C>G (HSD17B3) XP_011516921.1:n.524+395C>G
XM_017014671.1:c.524+395C>G (HSD17B3) XP_016870160.1:n.524+395C>G
XM_017014672.1:c.524+395C>G (HSD17B3) XP_016870161.1:n.524+395C>G
XM_017014673.2:c.488+395C>G (HSD17B3) XP_016870162.1:n.488+395C>G
XM_017014674.1:c.416+395C>G (HSD17B3) XP_016870163.1:n.416+395C>G
XM_017014675.1:c.362+395C>G (HSD17B3) XP_016870164.1:n.362+395C>G
XM_017014677.1:c.164+395C>G (HSD17B3) XP_016870166.1:n.164+395C>G
XM_024447529.1:c.362+395C>G (HSD17B3) XP_024303297.1:n.362+395C>G
XR_002956778.1:n.2958+395C>G (HSD17B3)