Canonical Allele Identifier: CA2674977103
Gene: HSD17B4 HGNC NCBI

Linked Data

gnomAD v4: 5-119452472-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119452472C>A , CM000667.2:g.119452472C>A GRCh38
NC_000005.9:g.118788167C>A , CM000667.1:g.118788167C>A GRCh37
NC_000005.8:g.118816066C>A NCBI36
NG_008182.1:g.5020C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000683936.1:c.-104C>A ENSP00000507721.1:n.-104C>A
ENST00000256216.10:c.-104C>A ENSP00000256216.6:n.-104C>A
NM_000414.3:c.-104C>A NP_000405.1:n.-104C>A
NM_001199292.1:c.-104C>A NP_001186221.1:n.-104C>A
NM_001292027.1:c.-241C>A NP_001278956.1:n.-241C>A
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