Canonical Allele Identifier: CA374126367
Gene: HSD17B3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.96298426T>G , CM000671.2:g.96298426T>G GRCh38
NC_000009.11:g.99060708T>G , CM000671.1:g.99060708T>G GRCh37
NC_000009.10:g.98100529T>G NCBI36
NG_008157.1:g.8727A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375262.4:c.191A>C ENSP00000364411.2:p.Tyr64Ser
ENST00000375263.8:c.191A>C MANE Select ENSP00000364412.3:p.Tyr64Ser
ENST00000463517.2:n.1000A>C
ENST00000464104.6:n.661A>C
ENST00000467499.6:c.191A>C ENSP00000498077.1:p.Tyr64Ser
ENST00000643789.1:c.2483A>C
ENST00000648146.1:c.191A>C ENSP00000497238.1:p.Tyr64Ser
ENST00000648332.1:c.191A>C ENSP00000497562.1:p.Tyr64Ser
ENST00000648799.1:c.191A>C ENSP00000498039.1:p.Tyr64Ser
ENST00000650005.1:c.191A>C ENSP00000498121.1:p.Tyr64Ser
ENST00000650386.1:c.191A>C ENSP00000497464.1:p.Tyr64Ser
ENST00000375262.3:c.191A>C ENSP00000364411.2:p.Tyr64Ser
ENST00000375263.7:c.191A>C ENSP00000364412.3:p.Tyr64Ser
NM_000197.1:c.191A>C NP_000188.1:p.Tyr64Ser
XM_006717095.2:c.191A>C XP_006717158.1:p.Tyr64Ser
XM_011518618.1:c.191A>C XP_011516920.1:p.Tyr64Ser
XM_011518619.1:c.191A>C XP_011516921.1:p.Tyr64Ser
XM_011518620.1:c.191A>C XP_011516922.1:p.Tyr64Ser
XM_011518621.1:c.191A>C XP_011516923.1:p.Tyr64Ser
NM_000197.2:c.191A>C MANE Select NP_000188.1:p.Tyr64Ser
XM_011518618.2:c.191A>C XP_011516920.1:p.Tyr64Ser
XM_011518619.2:c.191A>C XP_011516921.1:p.Tyr64Ser
XM_017014671.1:c.191A>C XP_016870160.1:p.Tyr64Ser
XM_017014672.1:c.191A>C XP_016870161.1:p.Tyr64Ser
XM_017014673.2:c.191A>C XP_016870162.1:p.Tyr64Ser
XM_017014674.1:c.191A>C XP_016870163.1:p.Tyr64Ser
XM_017014675.1:c.105A>C XP_016870164.1:p.Val35=
XM_017014677.1:c.-746A>C XP_016870166.1:n.-746A>C
XM_024447529.1:c.105A>C XP_024303297.1:p.Val35=
XR_002956778.1:n.2625A>C