Canonical Allele Identifier: CA2674977101
Gene: HSD17B4 HGNC NCBI

Linked Data

gnomAD v4: 5-119452467-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119452467C>T , CM000667.2:g.119452467C>T GRCh38
NC_000005.9:g.118788162C>T , CM000667.1:g.118788162C>T GRCh37
NC_000005.8:g.118816061C>T NCBI36
NG_008182.1:g.5015C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000683936.1:c.-109C>T ENSP00000507721.1:n.-109C>T
ENST00000256216.10:c.-109C>T ENSP00000256216.6:n.-109C>T
NM_000414.3:c.-109C>T NP_000405.1:n.-109C>T
NM_001199292.1:c.-109C>T NP_001186221.1:n.-109C>T
NM_001292027.1:c.-246C>T NP_001278956.1:n.-246C>T
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