Canonical Allele Identifier: CA125915164
Gene: HSD17B4 HGNC NCBI

Linked Data

dbSNP Id: rs987067912

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.119452534C>G , CM000667.2:g.119452534C>G GRCh38
NC_000005.9:g.118788229C>G , CM000667.1:g.118788229C>G GRCh37
NC_000005.8:g.118816128C>G NCBI36
NG_008182.1:g.5082C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000509514.6:c.-42C>G ENSP00000426272.2:n.-42C>G
ENST00000518349.6:c.-42C>G ENSP00000507185.1:n.-42C>G
ENST00000682445.1:c.-42C>G ENSP00000508061.1:n.-42C>G
ENST00000682996.1:c.-42C>G ENSP00000507792.1:n.-42C>G
ENST00000683371.1:c.-42C>G ENSP00000508376.1:n.-42C>G
ENST00000683390.1:n.7C>G
ENST00000683936.1:c.-42C>G ENSP00000507721.1:n.-42C>G
ENST00000683974.1:n.41C>G
ENST00000684214.1:c.-42C>G ENSP00000508071.1:n.-42C>G
ENST00000414835.7:c.-220C>G ENSP00000411960.3:n.-220C>G
ENST00000510025.7:c.-42C>G MANE Select ENSP00000424940.3:n.-42C>G
ENST00000646058.1:c.-42C>G ENSP00000493579.1:n.-42C>G
ENST00000646590.1:c.-42C>G ENSP00000494892.1:n.-42C>G
ENST00000256216.10:c.-42C>G ENSP00000256216.6:n.-42C>G
ENST00000442060.7:c.-42C>G ENSP00000390208.3:n.-42C>G
ENST00000511186.5:n.62C>G
ENST00000515235.6:n.19C>G
ENST00000515320.5:c.-42C>G ENSP00000424613.1:n.-42C>G
NM_000414.3:c.-42C>G NP_000405.1:n.-42C>G
NM_001199291.2:c.-220C>G NP_001186220.1:n.-220C>G
NM_001199292.1:c.-42C>G NP_001186221.1:n.-42C>G
NM_001292027.1:c.-179C>G NP_001278956.1:n.-179C>G
NM_001292028.1:c.-641C>G NP_001278957.1:n.-641C>G
NM_000414.4:c.-42C>G MANE Select NP_000405.1:n.-42C>G
NM_001199291.3:c.-220C>G NP_001186220.1:n.-220C>G
NM_001199292.2:c.-42C>G NP_001186221.1:n.-42C>G
NM_001292027.2:c.-179C>G NP_001278956.1:n.-179C>G
NM_001292028.2:c.-641C>G NP_001278957.1:n.-641C>G
NM_001374497.1:c.-42C>G NP_001361426.1:n.-42C>G
NM_001374498.1:c.-42C>G NP_001361427.1:n.-42C>G
NM_001374499.1:c.-575C>G NP_001361428.1:n.-575C>G
NM_001374500.1:c.-768C>G NP_001361429.1:n.-768C>G
NM_001374501.1:c.-641C>G NP_001361430.1:n.-641C>G
NM_001374502.1:c.-646C>G NP_001361431.1:n.-646C>G
NM_001374503.1:c.-711C>G NP_001361432.1:n.-711C>G
NR_164653.1:n.38C>G
NR_164654.1:n.38C>G