Canonical Allele Identifier: CA023861

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 52056
• ClinVar RCV Id: RCV000258315 ; RCV001379699 ; RCV002223776 ; RCV002362664
• dbSNP Id: rs397507841
• gnomAD v4: 13-32326617-A-G
• MyVariant Identifiers: chr13:g.32900754A>G (hg19) ; chr13:g.32326617A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32326617A>G , CM000675.2:g.32326617A>G	GRCh38
NC_000013.10:g.32900754A>G , CM000675.1:g.32900754A>G	GRCh37
NC_000013.9:g.31798754A>G	NCBI36
NG_012772.3:g.16138A>G , LRG_293:g.16138A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.631+4A>G	ENSP00000434898.2:n.631+4A>G
ENST00000528762.2:c.631+4A>G	ENSP00000433168.2:n.631+4A>G
ENST00000530893.7:c.262+4A>G	ENSP00000499438.2:n.262+4A>G
ENST00000665585.2:c.631+4A>G	ENSP00000499570.2:n.631+4A>G
ENST00000666593.2:c.631+4A>G	ENSP00000499256.2:n.631+4A>G
ENST00000700202.2:c.631+4A>G	ENSP00000514856.2:n.631+4A>G
ENST00000700200.1:n.506A>G
ENST00000700201.1:c.*410+4A>G	ENSP00000514855.1:n.*410+4A>G
ENST00000380152.8:c.631+4A>G MANE Select	ENSP00000369497.3:n.631+4A>G
ENST00000544455.6:c.631+4A>G	ENSP00000439902.1:n.631+4A>G
ENST00000614259.2:c.631+4A>G	ENSP00000506251.1:n.631+4A>G
ENST00000680887.1:c.631+4A>G	ENSP00000505508.1:n.631+4A>G
ENST00000380152.7:c.631+4A>G	ENSP00000369497.3:n.631+4A>G
ENST00000530893.6:n.829+4A>G
ENST00000544455.5:c.631+4A>G	ENSP00000439902.1:n.631+4A>G
ENST00000614259.1:n.631+4A>G
NM_000059.3:c.631+4A>G , LRG_293t1:c.631+4A>G	NP_000050.2:n.631+4A>G
XM_011535203.1:c.631+4A>G	XP_011533505.1:n.631+4A>G
XM_011535204.1:c.631+4A>G	XP_011533506.1:n.631+4A>G
XM_011535205.1:c.631+4A>G	XP_011533507.1:n.631+4A>G
NM_000059.4:c.631+4A>G MANE Select	NP_000050.3:n.631+4A>G