Canonical Allele Identifier: CA15773633
Gene: HMGB1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1045411

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30459095C>T , CM000675.2:g.30459095C>T GRCh38
NC_000013.9:g.29931232C>T NCBI36
NC_000013.10:g.31033232C>T , CM000675.1:g.31033232C>T GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000341423.9:c.*2262G>A ENSP00000345347.5:p.=
ENST00000405805.5:c.*2262G>A ENSP00000384678.1:p.=
NM_001313892.1:c.*2262G>A NP_001300821.1:p.=
NM_001313893.1:c.*2262G>A NP_001300822.1:p.=
NM_002128.4:c.*2262G>A
NM_002128.5:c.*2262G>A NP_002119.1:p.=