Canonical Allele Identifier: CA16621220

Gene: HMGB3

Linked Data

• ClinVar Variation Id: 418251
• ClinVar RCV Id: RCV000481016
• dbSNP Id: rs1064793149
• MyVariant Identifiers: chrX:g.150154164del (hg19) ; chrX:g.150985691del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.150985691del , CM000685.2:g.150985691del	GRCh38
NC_000023.10:g.150154164del , CM000685.1:g.150154164del	GRCh37
NC_000023.9:g.149904822del	NCBI36
NG_034209.1:g.10184del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325307.12:c.92del MANE Select	ENSP00000359393.3:p.Asn31ThrfsTer?
ENST00000325307.11:c.92del	ENSP00000359393.3:p.Asn31ThrfsTer?
ENST00000419110.5:c.92del	ENSP00000410354.1:p.Asn31ThrfsTer?
ENST00000430118.1:c.92del	ENSP00000417027.1:p.Asn31ThrfsTer?
ENST00000448905.6:c.92del	ENSP00000442758.1:p.Asn31ThrfsTer?
ENST00000455596.5:c.92del	ENSP00000405601.1:p.Asn31ThrfsTer?
NM_001301228.1:c.92del	NP_001288157.1:p.Asn31ThrfsTer?
NM_001301229.1:c.92del	NP_001288158.1:p.Asn31ThrfsTer?
NM_001301231.1:c.152del	NP_001288160.1:p.Asn51ThrfsTer?
NM_005342.3:c.92del	NP_005333.2:p.Asn31ThrfsTer?
XM_024452369.1:c.92del	XP_024308137.1:p.Asn31ThrfsTer?
NM_005342.4:c.92del MANE Select	NP_005333.2:p.Asn31ThrfsTer?
NM_001301229.2:c.92del	NP_001288158.1:p.Asn31ThrfsTer?
NM_001301231.2:c.152del	NP_001288160.1:p.Asn51ThrfsTer?
NM_001301228.2:c.92del	NP_001288157.1:p.Asn31ThrfsTer?