Canonical Allele Identifier: CA021988

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 184598
• ClinVar RCV Id: RCV000163880 ; RCV000485328 ; RCV000542286 ; RCV000662989
• dbSNP Id: rs786201560
• gnomAD v4: 13-32316512-C-T
• MyVariant Identifiers: chr13:g.32890649C>T (hg19) ; chr13:g.32316512C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32316512C>T , CM000675.2:g.32316512C>T	GRCh38
NC_000013.10:g.32890649C>T , CM000675.1:g.32890649C>T	GRCh37
NC_000013.9:g.31788649C>T	NCBI36
NG_012772.3:g.6033C>T , LRG_293:g.6033C>T
NG_017006.1:g.443G>A
NG_017006.2:g.3852G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.52C>T	ENSP00000434898.2:p.Arg18Cys
ENST00000528762.2:c.52C>T	ENSP00000433168.2:p.Arg18Cys
ENST00000530893.7:c.-314C>T	ENSP00000499438.2:n.-314C>T
ENST00000665585.2:c.52C>T	ENSP00000499570.2:p.Arg18Cys
ENST00000666593.2:c.52C>T	ENSP00000499256.2:p.Arg18Cys
ENST00000700202.2:c.52C>T	ENSP00000514856.2:p.Arg18Cys
ENST00000700199.1:n.176C>T
ENST00000700200.1:n.176C>T
ENST00000700201.1:c.52C>T	ENSP00000514855.1:p.Arg18Cys
ENST00000380152.8:c.52C>T MANE Select	ENSP00000369497.3:p.Arg18Cys
ENST00000544455.6:c.52C>T	ENSP00000439902.1:p.Arg18Cys
ENST00000614259.2:c.52C>T	ENSP00000506251.1:p.Arg18Cys
ENST00000680887.1:c.52C>T	ENSP00000505508.1:p.Arg18Cys
ENST00000380152.7:c.52C>T	ENSP00000369497.3:p.Arg18Cys
ENST00000530893.6:n.254C>T
ENST00000544455.5:c.52C>T	ENSP00000439902.1:p.Arg18Cys
ENST00000614259.1:n.52C>T
NM_000059.3:c.52C>T , LRG_293t1:c.52C>T	NP_000050.2:p.Arg18Cys
XM_011535203.1:c.52C>T	XP_011533505.1:p.Arg18Cys
XM_011535204.1:c.52C>T	XP_011533506.1:p.Arg18Cys
XM_011535205.1:c.52C>T	XP_011533507.1:p.Arg18Cys
NM_000059.4:c.52C>T MANE Select	NP_000050.3:p.Arg18Cys