Canonical Allele Identifier: CA658653813

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 441337
• ClinVar RCV Id: RCV000509999 ; RCV001072008
• dbSNP Id: rs1555286878
• MyVariant Identifiers: chr13:g.32936833A>C (hg19) ; chr13:g.32362696A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362696A>C , CM000675.2:g.32362696A>C	GRCh38
NC_000013.10:g.32936833A>C , CM000675.1:g.32936833A>C	GRCh37
NC_000013.9:g.31834833A>C	NCBI36
NG_012772.3:g.52217A>C , LRG_293:g.52217A>C

Transcript Alleles

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