Canonical Allele Identifier: CA387768169

Gene: BRCA2

Linked Data

• dbSNP Id: rs397507261
• MyVariant Identifiers: chr13:g.32972803C>A (hg19) ; chr13:g.32398666C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398666C>A , CM000675.2:g.32398666C>A	GRCh38
NC_000013.10:g.32972803C>A , CM000675.1:g.32972803C>A	GRCh37
NC_000013.9:g.31870803C>A	NCBI36
NG_012772.3:g.88187C>A , LRG_293:g.88187C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*676C>A	ENSP00000434898.2:n.*676C>A
ENST00000528762.2:c.*1520C>A	ENSP00000433168.2:n.*1520C>A
ENST00000530893.7:c.9784C>A	ENSP00000499438.2:p.Arg3262Ser
ENST00000665585.2:c.*1715C>A	ENSP00000499570.2:n.*1715C>A
ENST00000700202.2:c.10102C>A	ENSP00000514856.2:p.Arg3368Ser
ENST00000700202.1:c.2569C>A	ENSP00000514856.1:p.Arg857Ser
ENST00000700203.1:n.2280C>A
ENST00000380152.8:c.10153C>A MANE Select	ENSP00000369497.3:p.Arg3385Ser
ENST00000544455.6:c.10153C>A	ENSP00000439902.1:p.Arg3385Ser
ENST00000614259.2:c.10161C>A	ENSP00000506251.1:n.10161C>A
ENST00000680887.1:c.10153C>A	ENSP00000505508.1:p.Arg3385Ser
ENST00000380152.7:c.10153C>A	ENSP00000369497.3:p.Arg3385Ser
ENST00000544455.5:c.10153C>A	ENSP00000439902.1:p.Arg3385Ser
NM_000059.3:c.10153C>A , LRG_293t1:c.10153C>A	NP_000050.2:p.Arg3385Ser
XM_011535203.1:c.10153C>A	XP_011533505.1:p.Arg3385Ser
XM_011535204.1:c.10057C>A	XP_011533506.1:p.Arg3353Ser
NM_000059.4:c.10153C>A MANE Select	NP_000050.3:p.Arg3385Ser