Canonical Allele Identifier: CA1577006775
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119452448T= , CM000667.2:g.119452448T= GRCh38
NC_000005.9:g.118788143T= , CM000667.1:g.118788143T= GRCh37
NC_000005.8:g.118816042T= NCBI36
NG_008182.1:g.4996T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256216.10:c.-128T= ENSP00000256216.6:n.-128T=
NM_000414.3:c.-128T= NP_000405.1:n.-128T=
NM_001199292.1:c.-128T= NP_001186221.1:n.-128T=
NM_001292027.1:c.-265T= NP_001278956.1:n.-265T=