Canonical Allele Identifier: CA13828402

Gene: HMGB1

Linked Data

• dbSNP Id: rs2249825
• gnomAD v2: 13-31037903-G-C
• gnomAD v3: 13-30463766-G-C
• gnomAD v4: 13-30463766-G-C
• MyVariant Identifiers: chr13:g.31037903G>C (hg19) ; chr13:g.30463766G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30463766G>C , CM000675.2:g.30463766G>C	GRCh38
NC_000013.10:g.31037903G>C , CM000675.1:g.31037903G>C	GRCh37
NC_000013.9:g.29935903G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000341423.10:c.-14-72C>G MANE Select	ENSP00000345347.5:n.-14-72C>G
ENST00000326004.4:c.-14-72C>G	ENSP00000369904.1:n.-14-72C>G
ENST00000339872.8:c.-14-72C>G	ENSP00000343040.4:n.-14-72C>G
ENST00000341423.9:c.-14-72C>G	ENSP00000345347.5:n.-14-72C>G
ENST00000399489.5:c.-86C>G	ENSP00000382412.1:n.-86C>G
ENST00000399494.5:c.-14-72C>G	ENSP00000382417.1:n.-14-72C>G
ENST00000405805.5:c.-14-72C>G	ENSP00000384678.1:n.-14-72C>G
ENST00000468384.1:n.120-72C>G
NM_001313892.1:c.-14-72C>G	NP_001300821.1:n.-14-72C>G
NM_001313893.1:c.-14-72C>G	NP_001300822.1:n.-14-72C>G
NM_002128.4:c.-14-72C>G	NP_002119.1:n.-14-72C>G
NM_002128.5:c.-14-72C>G	NP_002119.1:n.-14-72C>G
XM_005266365.1:c.-14-72C>G	XP_005266422.1:n.-14-72C>G
XM_005266368.1:c.-14-72C>G	XP_005266425.1:n.-14-72C>G
XM_011535055.1:c.-14-72C>G	XP_011533357.1:n.-14-72C>G
XM_011535056.1:c.-14-72C>G	XP_011533358.1:n.-14-72C>G
XR_941568.1:n.143-72C>G
NM_001363661.1:c.-14-72C>G	NP_001350590.1:n.-14-72C>G
NM_002128.6:c.-14-72C>G	NP_002119.1:n.-14-72C>G
XM_024449340.1:c.-14-72C>G	XP_024305108.1:n.-14-72C>G
XM_024449341.1:c.-14-72C>G	XP_024305109.1:n.-14-72C>G
XM_024449342.1:c.-14-72C>G	XP_024305110.1:n.-14-72C>G
XM_024449343.1:c.-14-72C>G	XP_024305111.1:n.-14-72C>G
NM_002128.7:c.-14-72C>G MANE Select	NP_002119.1:n.-14-72C>G
NM_001370339.1:c.-14-72C>G	NP_001357268.1:n.-14-72C>G
NM_001370340.1:c.-14-72C>G	NP_001357269.1:n.-14-72C>G
NM_001370341.1:c.-14-72C>G	NP_001357270.1:n.-14-72C>G
NM_001313892.2:c.-14-72C>G	NP_001300821.1:n.-14-72C>G
NM_001363661.2:c.-14-72C>G	NP_001350590.1:n.-14-72C>G