Canonical Allele Identifier: CA247862767
Gene: HMGB1 HGNC NCBI

Linked Data

dbSNP Id: rs974533813
gnomAD v2: 13-31113529-C-T
gnomAD v3: 13-30539392-C-T
gnomAD v4: 13-30539392-C-T
MyVariant Identifiers: chr13:g.31113529C>T (hg19) chr13:g.30539392C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30539392C>T , CM000675.2:g.30539392C>T GRCh38
NC_000013.10:g.31113529C>T , CM000675.1:g.31113529C>T GRCh37
NC_000013.9:g.30011529C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405805.5:c.-14-75698G>A ENSP00000384678.1:n.-14-75698G>A
NM_001313893.1:c.-14-75698G>A NP_001300822.1:n.-14-75698G>A
XM_024449340.1:c.-14-75698G>A XP_024305108.1:n.-14-75698G>A
NM_001370340.1:c.-14-75698G>A NP_001357269.1:n.-14-75698G>A
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