Canonical Allele Identifier: CA025398

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 183981
• ClinVar RCV Id: RCV000163073 ; RCV000637317 ; RCV000765141
• dbSNP Id: rs143999963
• MyVariant Identifiers: chr13:g.32937346A>T (hg19) ; chr13:g.32363209A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32363209A>T , CM000675.2:g.32363209A>T	GRCh38
NC_000013.10:g.32937346A>T , CM000675.1:g.32937346A>T	GRCh37
NC_000013.9:g.31835346A>T	NCBI36
NG_012772.3:g.52730A>T , LRG_293:g.52730A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.8007A>T	ENSP00000434898.2:p.Arg2669Ser
ENST00000528762.2:c.8007A>T	ENSP00000433168.2:p.Arg2669Ser
ENST00000530893.7:c.7638A>T	ENSP00000499438.2:p.Arg2546Ser
ENST00000665585.2:c.8007A>T	ENSP00000499570.2:p.Arg2669Ser
ENST00000666593.2:c.8007A>T	ENSP00000499256.2:p.Arg2669Ser
ENST00000700202.2:c.8007A>T	ENSP00000514856.2:p.Arg2669Ser
ENST00000700202.1:c.474A>T	ENSP00000514856.1:p.Arg158Ser
ENST00000380152.8:c.8007A>T MANE Select	ENSP00000369497.3:p.Arg2669Ser
ENST00000544455.6:c.8007A>T	ENSP00000439902.1:p.Arg2669Ser
ENST00000614259.2:c.8015A>T	ENSP00000506251.1:n.8015A>T
ENST00000665585.1:c.572A>T
ENST00000680887.1:c.8007A>T	ENSP00000505508.1:p.Arg2669Ser
ENST00000380152.7:c.8007A>T	ENSP00000369497.3:p.Arg2669Ser
ENST00000544455.5:c.8007A>T	ENSP00000439902.1:p.Arg2669Ser
NM_000059.3:c.8007A>T , LRG_293t1:c.8007A>T	NP_000050.2:p.Arg2669Ser
XM_011535203.1:c.8007A>T	XP_011533505.1:p.Arg2669Ser
XM_011535204.1:c.7911A>T	XP_011533506.1:p.Arg2637Ser
XM_011535205.1:c.8007A>T	XP_011533507.1:p.Arg2669Ser
NM_000059.4:c.8007A>T MANE Select	NP_000050.3:p.Arg2669Ser