Canonical Allele Identifier: CA1577006786
Gene: HSD17B4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119452462A= , CM000667.2:g.119452462A= GRCh38
NC_000005.9:g.118788157A= , CM000667.1:g.118788157A= GRCh37
NC_000005.8:g.118816056A= NCBI36
NG_008182.1:g.5010A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256216.10:c.-114A= ENSP00000256216.6:n.-114A=
NM_000414.3:c.-114A= NP_000405.1:n.-114A=
NM_001199292.1:c.-114A= NP_001186221.1:n.-114A=
NM_001292027.1:c.-251A= NP_001278956.1:n.-251A=