Canonical Allele Identifier: CA025367

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 183947
• ClinVar RCV Id: RCV000162937 ; RCV000258212 ; RCV000496302 ; RCV000586885 ; RCV000637349
• dbSNP Id: rs786201180
• gnomAD v4: 13-32362698-G-A
• MyVariant Identifiers: chr13:g.32936835G>A (hg19) ; chr13:g.32362698G>A (hg38)
• PubMed: PMID:26187060 ; PMID:27157322

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362698G>A , CM000675.2:g.32362698G>A	GRCh38
NC_000013.10:g.32936835G>A , CM000675.1:g.32936835G>A	GRCh37
NC_000013.9:g.31834835G>A	NCBI36
NG_012772.3:g.52219G>A , LRG_293:g.52219G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7976+5G>A	ENSP00000434898.2:n.7976+5G>A
ENST00000528762.2:c.7976+5G>A	ENSP00000433168.2:n.7976+5G>A
ENST00000530893.7:c.7607+5G>A	ENSP00000499438.2:n.7607+5G>A
ENST00000665585.2:c.7976+5G>A	ENSP00000499570.2:n.7976+5G>A
ENST00000666593.2:c.7976+5G>A	ENSP00000499256.2:n.7976+5G>A
ENST00000700202.2:c.7976+5G>A	ENSP00000514856.2:n.7976+5G>A
ENST00000700202.1:c.443+5G>A	ENSP00000514856.1:n.443+5G>A
ENST00000380152.8:c.7976+5G>A MANE Select	ENSP00000369497.3:n.7976+5G>A
ENST00000544455.6:c.7976+5G>A	ENSP00000439902.1:n.7976+5G>A
ENST00000614259.2:c.7984+5G>A	ENSP00000506251.1:n.7984+5G>A
ENST00000665585.1:c.541+5G>A
ENST00000680887.1:c.7976+5G>A	ENSP00000505508.1:n.7976+5G>A
ENST00000380152.7:c.7976+5G>A	ENSP00000369497.3:n.7976+5G>A
ENST00000544455.5:c.7976+5G>A	ENSP00000439902.1:n.7976+5G>A
NM_000059.3:c.7976+5G>A , LRG_293t1:c.7976+5G>A	NP_000050.2:n.7976+5G>A
XM_011535203.1:c.7976+5G>A	XP_011533505.1:n.7976+5G>A
XM_011535204.1:c.7880+5G>A	XP_011533506.1:n.7880+5G>A
XM_011535205.1:c.7976+5G>A	XP_011533507.1:n.7976+5G>A
NM_000059.4:c.7976+5G>A MANE Select	NP_000050.3:n.7976+5G>A