Canonical Allele Identifier: CA1865974457
Gene: HSD17B3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.96235382C= , CM000671.2:g.96235382C= GRCh38
NC_000009.11:g.98997664C= , CM000671.1:g.98997664C= GRCh37
NC_000009.10:g.98037485C= NCBI36
NG_008157.1:g.71771G=

Transcript Alleles

HGVS Amino-acid change
ENST00000375263.8:c.*78G= MANE Select ENSP00000364412.3:n.*78G=
ENST00000463517.2:n.2553G=
ENST00000464104.6:n.1949G=
ENST00000467499.6:c.*710G= ENSP00000498077.1:n.*710G=
ENST00000494814.6:n.561G=
ENST00000643789.1:c.3303G=
ENST00000375262.3:c.*78G= ENSP00000364411.2:n.*78G=
ENST00000375263.7:c.*78G= ENSP00000364412.3:n.*78G=
ENST00000464104.5:n.864G=
ENST00000467499.5:n.271G=
ENST00000494814.5:n.570G=
NM_000197.1:c.*78G= NP_000188.1:n.*78G=
XM_005251970.3:c.*78G= XP_005252027.1:n.*78G=
XM_011518618.1:c.*78G= XP_011516920.1:n.*78G=
XM_011518619.1:c.*78G= XP_011516921.1:n.*78G=
XM_011518620.1:c.*78G= XP_011516922.1:n.*78G=
NM_000197.2:c.*78G= MANE Select NP_000188.1:n.*78G=
XM_011518618.2:c.*78G= XP_011516920.1:n.*78G=
XM_011518619.2:c.*78G= XP_011516921.1:n.*78G=
XM_017014671.1:c.*78G= XP_016870160.1:n.*78G=
XM_017014672.1:c.*78G= XP_016870161.1:n.*78G=
XM_017014673.2:c.*78G= XP_016870162.1:n.*78G=
XM_017014674.1:c.*78G= XP_016870163.1:n.*78G=
XM_017014675.1:c.*78G= XP_016870164.1:n.*78G=
XM_017014677.1:c.*78G= XP_016870166.1:n.*78G=
XM_024447529.1:c.*78G= XP_024303297.1:n.*78G=
XR_002956778.1:n.3483G=