Canonical Allele Identifier: CA1577006795
Gene: HSD17B4 HGNC NCBI

Linked Data

dbSNP Id: rs1580480340

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119452469A>G , CM000667.2:g.119452469A>G GRCh38
NC_000005.9:g.118788164A>G , CM000667.1:g.118788164A>G GRCh37
NC_000005.8:g.118816063A>G NCBI36
NG_008182.1:g.5017A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000683936.1:c.-107A>G ENSP00000507721.1:n.-107A>G
ENST00000256216.10:c.-107A>G ENSP00000256216.6:n.-107A>G
NM_000414.3:c.-107A>G NP_000405.1:n.-107A>G
NM_001199292.1:c.-107A>G NP_001186221.1:n.-107A>G
NM_001292027.1:c.-244A>G NP_001278956.1:n.-244A>G