Canonical Allele Identifier: CA954564277

Gene: HMGB1

Linked Data

• dbSNP Id: rs1868750646
• gnomAD v3: 13-30539304-A-G
• gnomAD v4: 13-30539304-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30539304A>G , CM000675.2:g.30539304A>G	GRCh38
NC_000013.10:g.31113441A>G , CM000675.1:g.31113441A>G	GRCh37
NC_000013.9:g.30011441A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405805.5:c.-14-75610T>C	ENSP00000384678.1:n.-14-75610T>C
NM_001313893.1:c.-14-75610T>C	NP_001300822.1:n.-14-75610T>C
XM_024449340.1:c.-14-75610T>C	XP_024305108.1:n.-14-75610T>C
NM_001370340.1:c.-14-75610T>C	NP_001357269.1:n.-14-75610T>C