Canonical Allele Identifier: CA2674977086
Gene: HSD17B4 HGNC NCBI

Linked Data

gnomAD v4: 5-119452446-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119452446C>A , CM000667.2:g.119452446C>A GRCh38
NC_000005.9:g.118788141C>A , CM000667.1:g.118788141C>A GRCh37
NC_000005.8:g.118816040C>A NCBI36
NG_008182.1:g.4994C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256216.10:c.-130C>A ENSP00000256216.6:n.-130C>A
NM_000414.3:c.-130C>A NP_000405.1:n.-130C>A
NM_001199292.1:c.-130C>A NP_001186221.1:n.-130C>A
NM_001292027.1:c.-267C>A NP_001278956.1:n.-267C>A
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