Canonical Allele Identifier: CA2229202878
Gene: HSF4 HGNC NCBI

Linked Data

dbSNP Id: rs2031105482

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67164668C>T , CM000678.2:g.67164668C>T GRCh38
NC_000016.9:g.67198571C>T , CM000678.1:g.67198571C>T GRCh37
NC_000016.8:g.65756072C>T NCBI36
NG_009294.1:g.6284C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518227.1:c.499C>T
ENST00000518753.5:c.295+524C>T
ENST00000523360.1:n.348C>T
ENST00000580114.5:c.822C>T
NM_001040667.2:c.-144C>T NP_001035757.1:n.-144C>T
NM_001538.3:c.-144C>T NP_001529.2:n.-144C>T
NM_001040667.3:c.-144C>T NP_001035757.1:n.-144C>T
NM_001538.4:c.-144C>T NP_001529.2:n.-144C>T