Canonical Allele Identifier: CA2081986134
Gene: HMGB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30539290C= , CM000675.2:g.30539290C= GRCh38
NC_000013.10:g.31113427C= , CM000675.1:g.31113427C= GRCh37
NC_000013.9:g.30011427C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000405805.5:c.-14-75596G= ENSP00000384678.1:n.-14-75596G=
NM_001313893.1:c.-14-75596G= NP_001300822.1:n.-14-75596G=
XM_024449340.1:c.-14-75596G= XP_024305108.1:n.-14-75596G=
NM_001370340.1:c.-14-75596G= NP_001357269.1:n.-14-75596G=
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