Canonical Allele Identifier: CA247862752
Gene: HMGB1 HGNC NCBI

Linked Data

dbSNP Id: rs528670663
gnomAD v2: 13-31113400-G-T
gnomAD v3: 13-30539263-G-T
gnomAD v4: 13-30539263-G-T
MyVariant Identifiers: chr13:g.31113400G>T (hg19) chr13:g.30539263G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30539263G>T , CM000675.2:g.30539263G>T GRCh38
NC_000013.10:g.31113400G>T , CM000675.1:g.31113400G>T GRCh37
NC_000013.9:g.30011400G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000405805.5:c.-14-75569C>A ENSP00000384678.1:n.-14-75569C>A
NM_001313893.1:c.-14-75569C>A NP_001300822.1:n.-14-75569C>A
XM_024449340.1:c.-14-75569C>A XP_024305108.1:n.-14-75569C>A
NM_001370340.1:c.-14-75569C>A NP_001357269.1:n.-14-75569C>A
Search 100 bp 5'
Search 100 bp 3'