Canonical Allele Identifier: CA697205710

Gene: HMGB1

Linked Data

• dbSNP Id: rs1198448492
• MyVariant Identifiers: chr13:g.31113493T>C (hg19) ; chr13:g.30539356T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30539356T>C , CM000675.2:g.30539356T>C	GRCh38
NC_000013.10:g.31113493T>C , CM000675.1:g.31113493T>C	GRCh37
NC_000013.9:g.30011493T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405805.5:c.-14-75662A>G	ENSP00000384678.1:n.-14-75662A>G
NM_001313893.1:c.-14-75662A>G	NP_001300822.1:n.-14-75662A>G
XM_024449340.1:c.-14-75662A>G	XP_024305108.1:n.-14-75662A>G
NM_001370340.1:c.-14-75662A>G	NP_001357269.1:n.-14-75662A>G