Canonical Allele Identifier: CA1577006790
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119452466G= , CM000667.2:g.119452466G= GRCh38
NC_000005.9:g.118788161G= , CM000667.1:g.118788161G= GRCh37
NC_000005.8:g.118816060G= NCBI36
NG_008182.1:g.5014G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000683936.1:c.-110G= ENSP00000507721.1:n.-110G=
ENST00000256216.10:c.-110G= ENSP00000256216.6:n.-110G=
NM_000414.3:c.-110G= NP_000405.1:n.-110G=
NM_001199292.1:c.-110G= NP_001186221.1:n.-110G=
NM_001292027.1:c.-247G= NP_001278956.1:n.-247G=