Canonical Allele Identifier: CA2081986119
Gene: HMGB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30539276T= , CM000675.2:g.30539276T= GRCh38
NC_000013.10:g.31113413T= , CM000675.1:g.31113413T= GRCh37
NC_000013.9:g.30011413T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405805.5:c.-14-75582A= ENSP00000384678.1:n.-14-75582A=
NM_001313893.1:c.-14-75582A= NP_001300822.1:n.-14-75582A=
XM_024449340.1:c.-14-75582A= XP_024305108.1:n.-14-75582A=
NM_001370340.1:c.-14-75582A= NP_001357269.1:n.-14-75582A=