Canonical Allele Identifier: CA387754878

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 462492
• ClinVar RCV Id: RCV000549352 ; RCV000781131 ; RCV000777215 ; RCV003483662
• dbSNP Id: rs1555288163
• gnomAD v4: 13-32376741-G-A
• MyVariant Identifiers: chr13:g.32950878G>A (hg19) ; chr13:g.32376741G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376741G>A , CM000675.2:g.32376741G>A	GRCh38
NC_000013.10:g.32950878G>A , CM000675.1:g.32950878G>A	GRCh37
NC_000013.9:g.31848878G>A	NCBI36
NG_012772.3:g.66262G>A , LRG_293:g.66262G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8704G>A	ENSP00000434898.2:p.Ala2902Thr
ENST00000528762.2:c.*71G>A	ENSP00000433168.2:n.*71G>A
ENST00000530893.7:c.8335G>A	ENSP00000499438.2:p.Ala2779Thr
ENST00000665585.2:c.*266G>A	ENSP00000499570.2:n.*266G>A
ENST00000666593.2:c.8704G>A	ENSP00000499256.2:p.Ala2902Thr
ENST00000700202.2:c.8704G>A	ENSP00000514856.2:p.Ala2902Thr
ENST00000700202.1:c.1171G>A	ENSP00000514856.1:p.Ala391Thr
ENST00000700203.1:n.831G>A
ENST00000380152.8:c.8704G>A MANE Select	ENSP00000369497.3:p.Ala2902Thr
ENST00000544455.6:c.8704G>A	ENSP00000439902.1:p.Ala2902Thr
ENST00000614259.2:c.8712G>A	ENSP00000506251.1:n.8712G>A
ENST00000665585.1:c.1582G>A
ENST00000680887.1:c.8704G>A	ENSP00000505508.1:p.Ala2902Thr
ENST00000380152.7:c.8704G>A	ENSP00000369497.3:p.Ala2902Thr
ENST00000528762.1:c.266G>A	ENSP00000433168.1:n.266G>A
ENST00000544455.5:c.8704G>A	ENSP00000439902.1:p.Ala2902Thr
NM_000059.3:c.8704G>A , LRG_293t1:c.8704G>A	NP_000050.2:p.Ala2902Thr
XM_011535203.1:c.8704G>A	XP_011533505.1:p.Ala2902Thr
XM_011535204.1:c.8608G>A	XP_011533506.1:p.Ala2870Thr
XM_011535205.1:c.8704G>A	XP_011533507.1:p.Ala2902Thr
NM_000059.4:c.8704G>A MANE Select	NP_000050.3:p.Ala2902Thr