Canonical Allele Identifier: CA1577006776
Gene: HSD17B4 HGNC NCBI

Linked Data

dbSNP Id: rs1754129788
gnomAD v4: 5-119452448-T-A
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Genomic Alleles

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

Transcript Alleles

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