Canonical Allele Identifier: CA387763878

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 634724
• ClinVar RCV Id: RCV000785376
• dbSNP Id: rs1566260318
• MyVariant Identifiers: chr13:g.32971183T>C (hg19) ; chr13:g.32397046T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32397046T>C , CM000675.2:g.32397046T>C	GRCh38
NC_000013.10:g.32971183T>C , CM000675.1:g.32971183T>C	GRCh37
NC_000013.9:g.31869183T>C	NCBI36
NG_012772.3:g.86567T>C , LRG_293:g.86567T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*171+2T>C	ENSP00000434898.2:n.*171+2T>C
ENST00000528762.2:c.*1015+2T>C	ENSP00000433168.2:n.*1015+2T>C
ENST00000530893.7:c.9279+2T>C	ENSP00000499438.2:n.9279+2T>C
ENST00000665585.2:c.*1210+2T>C	ENSP00000499570.2:n.*1210+2T>C
ENST00000700202.2:c.9597+2T>C	ENSP00000514856.2:n.9597+2T>C
ENST00000700202.1:c.2064+2T>C	ENSP00000514856.1:n.2064+2T>C
ENST00000700203.1:n.1775+2T>C
ENST00000380152.8:c.9648+2T>C MANE Select	ENSP00000369497.3:n.9648+2T>C
ENST00000544455.6:c.9648+2T>C	ENSP00000439902.1:n.9648+2T>C
ENST00000614259.2:c.9656+2T>C	ENSP00000506251.1:n.9656+2T>C
ENST00000665585.1:c.2526+2T>C
ENST00000680887.1:c.9648+2T>C	ENSP00000505508.1:n.9648+2T>C
ENST00000380152.7:c.9648+2T>C	ENSP00000369497.3:n.9648+2T>C
ENST00000470094.1:c.731+2T>C
ENST00000533776.1:n.236+2T>C
ENST00000544455.5:c.9648+2T>C	ENSP00000439902.1:n.9648+2T>C
NM_000059.3:c.9648+2T>C , LRG_293t1:c.9648+2T>C	NP_000050.2:n.9648+2T>C
XM_011535203.1:c.9648+2T>C	XP_011533505.1:n.9648+2T>C
XM_011535204.1:c.9552+2T>C	XP_011533506.1:n.9552+2T>C
NM_000059.4:c.9648+2T>C MANE Select	NP_000050.3:n.9648+2T>C