Canonical Allele Identifier: CA2081916994
Gene: HMGB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30459172A= , CM000675.2:g.30459172A= GRCh38
NC_000013.10:g.31033309A= , CM000675.1:g.31033309A= GRCh37
NC_000013.9:g.29931309A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000341423.10:c.*2185T= MANE Select ENSP00000345347.5:n.*2185T=
ENST00000341423.9:c.*2185T= ENSP00000345347.5:n.*2185T=
ENST00000405805.5:c.*2185T= ENSP00000384678.1:n.*2185T=
NM_001313892.1:c.*2185T= NP_001300821.1:n.*2185T=
NM_001313893.1:c.*2185T= NP_001300822.1:n.*2185T=
NM_002128.4:c.*2185T= NP_002119.1:n.*2185T=
NM_002128.5:c.*2185T= NP_002119.1:n.*2185T=
NM_001363661.1:c.*2406T= NP_001350590.1:n.*2406T=
NM_002128.6:c.*2185T= NP_002119.1:n.*2185T=
NM_002128.7:c.*2185T= MANE Select NP_002119.1:n.*2185T=
NM_001370339.1:c.*2511T= NP_001357268.1:n.*2511T=
NM_001370340.1:c.*2185T= NP_001357269.1:n.*2185T=
NM_001370341.1:c.*2185T= NP_001357270.1:n.*2185T=
NM_001313892.2:c.*2185T= NP_001300821.1:n.*2185T=
NM_001363661.2:c.*2406T= NP_001350590.1:n.*2406T=