Canonical Allele Identifier: CA2081986114
Gene: HMGB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30539273T= , CM000675.2:g.30539273T= GRCh38
NC_000013.10:g.31113410T= , CM000675.1:g.31113410T= GRCh37
NC_000013.9:g.30011410T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000405805.5:c.-14-75579A= ENSP00000384678.1:n.-14-75579A=
NM_001313893.1:c.-14-75579A= NP_001300822.1:n.-14-75579A=
XM_024449340.1:c.-14-75579A= XP_024305108.1:n.-14-75579A=
NM_001370340.1:c.-14-75579A= NP_001357269.1:n.-14-75579A=
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