Canonical Allele Identifier: CA697205736
Gene: HMGB1 HGNC NCBI

Linked Data

dbSNP Id: rs1383192012
gnomAD v3: 13-30539391-T-C
gnomAD v4: 13-30539391-T-C
MyVariant Identifiers: chr13:g.31113528T>C (hg19) chr13:g.30539391T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30539391T>C , CM000675.2:g.30539391T>C GRCh38
NC_000013.10:g.31113528T>C , CM000675.1:g.31113528T>C GRCh37
NC_000013.9:g.30011528T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405805.5:c.-14-75697A>G ENSP00000384678.1:n.-14-75697A>G
NM_001313893.1:c.-14-75697A>G NP_001300822.1:n.-14-75697A>G
XM_024449340.1:c.-14-75697A>G XP_024305108.1:n.-14-75697A>G
NM_001370340.1:c.-14-75697A>G NP_001357269.1:n.-14-75697A>G
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