Canonical Allele Identifier: CA025895

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 52712
• ClinVar RCV Id: RCV000114023 ; RCV001018542 ; RCV001366157
• dbSNP Id: rs81002844
• MyVariant Identifiers: chr13:g.32953884C>G (hg19) ; chr13:g.32379747C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379747C>G , CM000675.2:g.32379747C>G	GRCh38
NC_000013.10:g.32953884C>G , CM000675.1:g.32953884C>G	GRCh37
NC_000013.9:g.31851884C>G	NCBI36
NG_012772.3:g.69268C>G , LRG_293:g.69268C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8954-3C>G	ENSP00000434898.2:n.8954-3C>G
ENST00000528762.2:c.*321-3C>G	ENSP00000433168.2:n.*321-3C>G
ENST00000530893.7:c.8585-3C>G	ENSP00000499438.2:n.8585-3C>G
ENST00000665585.2:c.*516-3C>G	ENSP00000499570.2:n.*516-3C>G
ENST00000666593.2:c.8954-3C>G	ENSP00000499256.2:n.8954-3C>G
ENST00000700202.2:c.8954-54C>G	ENSP00000514856.2:n.8954-54C>G
ENST00000700202.1:c.1421-54C>G	ENSP00000514856.1:n.1421-54C>G
ENST00000700203.1:n.1081-3C>G
ENST00000380152.8:c.8954-3C>G MANE Select	ENSP00000369497.3:n.8954-3C>G
ENST00000544455.6:c.8954-3C>G	ENSP00000439902.1:n.8954-3C>G
ENST00000614259.2:c.8962-3C>G	ENSP00000506251.1:n.8962-3C>G
ENST00000665585.1:c.1832-3C>G
ENST00000680887.1:c.8954-3C>G	ENSP00000505508.1:n.8954-3C>G
ENST00000380152.7:c.8954-3C>G	ENSP00000369497.3:n.8954-3C>G
ENST00000544455.5:c.8954-3C>G	ENSP00000439902.1:n.8954-3C>G
NM_000059.3:c.8954-3C>G , LRG_293t1:c.8954-3C>G	NP_000050.2:n.8954-3C>G
XM_011535203.1:c.8954-3C>G	XP_011533505.1:n.8954-3C>G
XM_011535204.1:c.8858-3C>G	XP_011533506.1:n.8858-3C>G
XM_011535205.1:c.8755-3C>G	XP_011533507.1:n.8755-3C>G
NM_000059.4:c.8954-3C>G MANE Select	NP_000050.3:n.8954-3C>G