Canonical Allele Identifier: CA025559

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 142807
• ClinVar RCV Id: RCV000132229 ; RCV000220276 ; RCV000539628 ; RCV000766316 ; RCV001353839 ; RCV003462040
• dbSNP Id: rs587782732
• gnomAD v4: 13-32363505-T-A
• MyVariant Identifiers: chr13:g.32937642T>A (hg19) ; chr13:g.32363505T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32363505T>A , CM000675.2:g.32363505T>A	GRCh38
NC_000013.10:g.32937642T>A , CM000675.1:g.32937642T>A	GRCh37
NC_000013.9:g.31835642T>A	NCBI36
NG_012772.3:g.53026T>A , LRG_293:g.53026T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8303T>A	ENSP00000434898.2:p.Leu2768His
ENST00000528762.2:c.8303T>A	ENSP00000433168.2:p.Leu2768His
ENST00000530893.7:c.7934T>A	ENSP00000499438.2:p.Leu2645His
ENST00000665585.2:c.8303T>A	ENSP00000499570.2:p.Leu2768His
ENST00000666593.2:c.8303T>A	ENSP00000499256.2:p.Leu2768His
ENST00000700202.2:c.8303T>A	ENSP00000514856.2:p.Leu2768His
ENST00000700202.1:c.770T>A	ENSP00000514856.1:p.Leu257His
ENST00000380152.8:c.8303T>A MANE Select	ENSP00000369497.3:p.Leu2768His
ENST00000544455.6:c.8303T>A	ENSP00000439902.1:p.Leu2768His
ENST00000614259.2:c.8311T>A	ENSP00000506251.1:n.8311T>A
ENST00000665585.1:c.868T>A
ENST00000680887.1:c.8303T>A	ENSP00000505508.1:p.Leu2768His
ENST00000380152.7:c.8303T>A	ENSP00000369497.3:p.Leu2768His
ENST00000544455.5:c.8303T>A	ENSP00000439902.1:p.Leu2768His
NM_000059.3:c.8303T>A , LRG_293t1:c.8303T>A	NP_000050.2:p.Leu2768His
XM_011535203.1:c.8303T>A	XP_011533505.1:p.Leu2768His
XM_011535204.1:c.8207T>A	XP_011533506.1:p.Leu2736His
XM_011535205.1:c.8303T>A	XP_011533507.1:p.Leu2768His
NM_000059.4:c.8303T>A MANE Select	NP_000050.3:p.Leu2768His