Canonical Allele Identifier: CA247853762

Gene: HMGB1

Linked Data

• dbSNP Id: rs779526016
• MyVariant Identifiers: chr13:g.31033197T>G (hg19) ; chr13:g.30459060T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30459060T>G , CM000675.2:g.30459060T>G	GRCh38
NC_000013.10:g.31033197T>G , CM000675.1:g.31033197T>G	GRCh37
NC_000013.9:g.29931197T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341423.10:c.*2297A>C MANE Select	ENSP00000345347.5:n.*2297A>C
ENST00000341423.9:c.*2297A>C	ENSP00000345347.5:n.*2297A>C
ENST00000405805.5:c.*2297A>C	ENSP00000384678.1:n.*2297A>C
NM_001313892.1:c.*2297A>C	NP_001300821.1:n.*2297A>C
NM_001313893.1:c.*2297A>C	NP_001300822.1:n.*2297A>C
NM_002128.4:c.*2297A>C	NP_002119.1:n.*2297A>C
NM_002128.5:c.*2297A>C	NP_002119.1:n.*2297A>C
NM_001363661.1:c.*2518A>C	NP_001350590.1:n.*2518A>C
NM_002128.6:c.*2297A>C	NP_002119.1:n.*2297A>C
NM_002128.7:c.*2297A>C MANE Select	NP_002119.1:n.*2297A>C
NM_001370339.1:c.*2623A>C	NP_001357268.1:n.*2623A>C
NM_001370340.1:c.*2297A>C	NP_001357269.1:n.*2297A>C
NM_001370341.1:c.*2297A>C	NP_001357270.1:n.*2297A>C
NM_001313892.2:c.*2297A>C	NP_001300821.1:n.*2297A>C
NM_001363661.2:c.*2518A>C	NP_001350590.1:n.*2518A>C