Canonical Allele Identifier: CA2674977118

Gene: HSD17B4

Linked Data

• gnomAD v4: 5-119452483-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119452483G>T , CM000667.2:g.119452483G>T	GRCh38
NC_000005.9:g.118788178G>T , CM000667.1:g.118788178G>T	GRCh37
NC_000005.8:g.118816077G>T	NCBI36
NG_008182.1:g.5031G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.-93G>T	ENSP00000426272.2:n.-93G>T
ENST00000682996.1:c.-93G>T	ENSP00000507792.1:n.-93G>T
ENST00000683936.1:c.-93G>T	ENSP00000507721.1:n.-93G>T
ENST00000684214.1:c.-93G>T	ENSP00000508071.1:n.-93G>T
ENST00000256216.10:c.-93G>T	ENSP00000256216.6:n.-93G>T
ENST00000511186.5:n.11G>T
NM_000414.3:c.-93G>T	NP_000405.1:n.-93G>T
NM_001199292.1:c.-93G>T	NP_001186221.1:n.-93G>T
NM_001292027.1:c.-230G>T	NP_001278956.1:n.-230G>T