Canonical Allele Identifier: CA609325535
Gene: HMGB1 HGNC NCBI

Linked Data

dbSNP Id: rs1180093105

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30539205A>C , CM000675.2:g.30539205A>C GRCh38
NC_000013.10:g.31113342A>C , CM000675.1:g.31113342A>C GRCh37
NC_000013.9:g.30011342A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405805.5:c.-14-75511T>G ENSP00000384678.1:n.-14-75511T>G
NM_001313893.1:c.-14-75511T>G NP_001300822.1:n.-14-75511T>G
XM_024449340.1:c.-14-75511T>G XP_024305108.1:n.-14-75511T>G
NM_001370340.1:c.-14-75511T>G NP_001357269.1:n.-14-75511T>G