Canonical Allele Identifier: CA1577006780
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119452453C= , CM000667.2:g.119452453C= GRCh38
NC_000005.9:g.118788148C= , CM000667.1:g.118788148C= GRCh37
NC_000005.8:g.118816047C= NCBI36
NG_008182.1:g.5001C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256216.10:c.-123C= ENSP00000256216.6:n.-123C=
NM_000414.3:c.-123C= NP_000405.1:n.-123C=
NM_001199292.1:c.-123C= NP_001186221.1:n.-123C=
NM_001292027.1:c.-260C= NP_001278956.1:n.-260C=