Canonical Allele Identifier: CA2081986070
Gene: HMGB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30539227C= , CM000675.2:g.30539227C= GRCh38
NC_000013.10:g.31113364C= , CM000675.1:g.31113364C= GRCh37
NC_000013.9:g.30011364C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405805.5:c.-14-75533G= ENSP00000384678.1:n.-14-75533G=
NM_001313893.1:c.-14-75533G= NP_001300822.1:n.-14-75533G=
XM_024449340.1:c.-14-75533G= XP_024305108.1:n.-14-75533G=
NM_001370340.1:c.-14-75533G= NP_001357269.1:n.-14-75533G=