Canonical Allele Identifier: CA2081986174
Gene: HMGB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30539321T= , CM000675.2:g.30539321T= GRCh38
NC_000013.10:g.31113458T= , CM000675.1:g.31113458T= GRCh37
NC_000013.9:g.30011458T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405805.5:c.-14-75627A= ENSP00000384678.1:n.-14-75627A=
NM_001313893.1:c.-14-75627A= NP_001300822.1:n.-14-75627A=
XM_024449340.1:c.-14-75627A= XP_024305108.1:n.-14-75627A=
NM_001370340.1:c.-14-75627A= NP_001357269.1:n.-14-75627A=