Canonical Allele Identifier: CA723022121
Gene: HSF4 HGNC NCBI

Linked Data

dbSNP Id: rs1273230299
MyVariant Identifiers: chr16:g.67198562G>A (hg19) chr16:g.67164659G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67164659G>A , CM000678.2:g.67164659G>A GRCh38
NC_000016.9:g.67198562G>A , CM000678.1:g.67198562G>A GRCh37
NC_000016.8:g.65756063G>A NCBI36
NG_009294.1:g.6275G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000518227.1:c.490G>A
ENST00000518753.5:c.295+515G>A
ENST00000523360.1:n.339G>A
ENST00000580114.5:c.813G>A
NM_001040667.2:c.-153G>A NP_001035757.1:n.-153G>A
NM_001538.3:c.-153G>A NP_001529.2:n.-153G>A
NM_001040667.3:c.-153G>A NP_001035757.1:n.-153G>A
NM_001538.4:c.-153G>A NP_001529.2:n.-153G>A
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