Canonical Allele Identifier: CA609325538
Gene: HMGB1 HGNC NCBI

Linked Data

dbSNP Id: rs1324116787
gnomAD v2: 13-31113451-C-T
gnomAD v3: 13-30539314-C-T
gnomAD v4: 13-30539314-C-T
MyVariant Identifiers: chr13:g.31113451C>T (hg19) chr13:g.30539314C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30539314C>T , CM000675.2:g.30539314C>T GRCh38
NC_000013.10:g.31113451C>T , CM000675.1:g.31113451C>T GRCh37
NC_000013.9:g.30011451C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000405805.5:c.-14-75620G>A ENSP00000384678.1:n.-14-75620G>A
NM_001313893.1:c.-14-75620G>A NP_001300822.1:n.-14-75620G>A
XM_024449340.1:c.-14-75620G>A XP_024305108.1:n.-14-75620G>A
NM_001370340.1:c.-14-75620G>A NP_001357269.1:n.-14-75620G>A
Search 100 bp 5'
Search 100 bp 3'