Canonical Allele Identifier: CA247862736
Gene: HMGB1 HGNC NCBI

Linked Data

dbSNP Id: rs1038797937
gnomAD v2: 13-31113314-G-A
gnomAD v3: 13-30539177-G-A
gnomAD v4: 13-30539177-G-A
MyVariant Identifiers: chr13:g.31113314G>A (hg19) chr13:g.30539177G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30539177G>A , CM000675.2:g.30539177G>A GRCh38
NC_000013.10:g.31113314G>A , CM000675.1:g.31113314G>A GRCh37
NC_000013.9:g.30011314G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405805.5:c.-14-75483C>T ENSP00000384678.1:n.-14-75483C>T
NM_001313893.1:c.-14-75483C>T NP_001300822.1:n.-14-75483C>T
XM_024449340.1:c.-14-75483C>T XP_024305108.1:n.-14-75483C>T
NM_001370340.1:c.-14-75483C>T NP_001357269.1:n.-14-75483C>T
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