Canonical Allele Identifier: CA125915036

Gene: HSD17B4

Linked Data

• dbSNP Id: rs972324798
• gnomAD v4: 5-119452489-C-T
• MyVariant Identifiers: chr5:g.118788184C>T (hg19) ; chr5:g.119452489C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119452489C>T , CM000667.2:g.119452489C>T	GRCh38
NC_000005.9:g.118788184C>T , CM000667.1:g.118788184C>T	GRCh37
NC_000005.8:g.118816083C>T	NCBI36
NG_008182.1:g.5037C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.-87C>T	ENSP00000426272.2:n.-87C>T
ENST00000682996.1:c.-87C>T	ENSP00000507792.1:n.-87C>T
ENST00000683936.1:c.-87C>T	ENSP00000507721.1:n.-87C>T
ENST00000684214.1:c.-87C>T	ENSP00000508071.1:n.-87C>T
ENST00000256216.10:c.-87C>T	ENSP00000256216.6:n.-87C>T
ENST00000511186.5:n.17C>T
NM_000414.3:c.-87C>T	NP_000405.1:n.-87C>T
NM_001199292.1:c.-87C>T	NP_001186221.1:n.-87C>T
NM_001292027.1:c.-224C>T	NP_001278956.1:n.-224C>T