Canonical Allele Identifier: CA2081986254
Gene: HMGB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30539370T= , CM000675.2:g.30539370T= GRCh38
NC_000013.10:g.31113507T= , CM000675.1:g.31113507T= GRCh37
NC_000013.9:g.30011507T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405805.5:c.-14-75676A= ENSP00000384678.1:n.-14-75676A=
NM_001313893.1:c.-14-75676A= NP_001300822.1:n.-14-75676A=
XM_024449340.1:c.-14-75676A= XP_024305108.1:n.-14-75676A=
NM_001370340.1:c.-14-75676A= NP_001357269.1:n.-14-75676A=