Canonical Allele Identifier: CA247862738
Gene: HMGB1 HGNC NCBI

Linked Data

dbSNP Id: rs143551920
gnomAD v2: 13-31113316-A-G
gnomAD v3: 13-30539179-A-G
gnomAD v4: 13-30539179-A-G
MyVariant Identifiers: chr13:g.31113316A>G (hg19) chr13:g.30539179A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30539179A>G , CM000675.2:g.30539179A>G GRCh38
NC_000013.10:g.31113316A>G , CM000675.1:g.31113316A>G GRCh37
NC_000013.9:g.30011316A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405805.5:c.-14-75485T>C ENSP00000384678.1:n.-14-75485T>C
NM_001313893.1:c.-14-75485T>C NP_001300822.1:n.-14-75485T>C
XM_024449340.1:c.-14-75485T>C XP_024305108.1:n.-14-75485T>C
NM_001370340.1:c.-14-75485T>C NP_001357269.1:n.-14-75485T>C
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