Canonical Allele Identifier: CA15773633
Gene: HMGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1250264
ClinVar RCV Id: RCV001652514
dbSNP Id: rs1045411

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000341423.10:c.*2262G>A MANE Select ENSP00000345347.5:n.*2262G>A
ENST00000341423.9:c.*2262G>A ENSP00000345347.5:n.*2262G>A
ENST00000405805.5:c.*2262G>A ENSP00000384678.1:n.*2262G>A
NM_001313892.1:c.*2262G>A NP_001300821.1:n.*2262G>A
NM_001313893.1:c.*2262G>A NP_001300822.1:n.*2262G>A
NM_002128.4:c.*2262G>A NP_002119.1:n.*2262G>A
NM_002128.5:c.*2262G>A NP_002119.1:n.*2262G>A
NM_001363661.1:c.*2483G>A NP_001350590.1:n.*2483G>A
NM_002128.6:c.*2262G>A NP_002119.1:n.*2262G>A
NM_002128.7:c.*2262G>A MANE Select NP_002119.1:n.*2262G>A
NM_001370339.1:c.*2588G>A NP_001357268.1:n.*2588G>A
NM_001370340.1:c.*2262G>A NP_001357269.1:n.*2262G>A
NM_001370341.1:c.*2262G>A NP_001357270.1:n.*2262G>A
NM_001313892.2:c.*2262G>A NP_001300821.1:n.*2262G>A
NM_001363661.2:c.*2483G>A NP_001350590.1:n.*2483G>A