Canonical Allele Identifier: CA125914999
Gene: HSD17B4 HGNC NCBI

Linked Data

dbSNP Id: rs1002219042

Genomic Alleles

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

Transcript Alleles

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