Canonical Allele Identifier: CA2081986105
Gene: HMGB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30539263G= , CM000675.2:g.30539263G= GRCh38
NC_000013.10:g.31113400G= , CM000675.1:g.31113400G= GRCh37
NC_000013.9:g.30011400G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000405805.5:c.-14-75569C= ENSP00000384678.1:n.-14-75569C=
NM_001313893.1:c.-14-75569C= NP_001300822.1:n.-14-75569C=
XM_024449340.1:c.-14-75569C= XP_024305108.1:n.-14-75569C=
NM_001370340.1:c.-14-75569C= NP_001357269.1:n.-14-75569C=
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