Canonical Allele Identifier: CA387757515

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 479304
• ClinVar RCV Id: RCV000570012 ; RCV002298665 ; RCV003318596 ; RCV001375531
• dbSNP Id: rs1555288470
• MyVariant Identifiers: chr13:g.32953970A>G (hg19) ; chr13:g.32379833A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379833A>G , CM000675.2:g.32379833A>G	GRCh38
NC_000013.10:g.32953970A>G , CM000675.1:g.32953970A>G	GRCh37
NC_000013.9:g.31851970A>G	NCBI36
NG_012772.3:g.69354A>G , LRG_293:g.69354A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.9037A>G	ENSP00000434898.2:p.Thr3013Ala
ENST00000528762.2:c.*404A>G	ENSP00000433168.2:n.*404A>G
ENST00000530893.7:c.8668A>G	ENSP00000499438.2:p.Thr2890Ala
ENST00000665585.2:c.*599A>G	ENSP00000499570.2:n.*599A>G
ENST00000666593.2:c.9037A>G	ENSP00000499256.2:p.Thr3013Ala
ENST00000700202.2:c.8986A>G	ENSP00000514856.2:p.Thr2996Ala
ENST00000700202.1:c.1453A>G	ENSP00000514856.1:p.Thr485Ala
ENST00000700203.1:n.1164A>G
ENST00000380152.8:c.9037A>G MANE Select	ENSP00000369497.3:p.Thr3013Ala
ENST00000544455.6:c.9037A>G	ENSP00000439902.1:p.Thr3013Ala
ENST00000614259.2:c.9045A>G	ENSP00000506251.1:n.9045A>G
ENST00000665585.1:c.1915A>G
ENST00000680887.1:c.9037A>G	ENSP00000505508.1:p.Thr3013Ala
ENST00000380152.7:c.9037A>G	ENSP00000369497.3:p.Thr3013Ala
ENST00000544455.5:c.9037A>G	ENSP00000439902.1:p.Thr3013Ala
NM_000059.3:c.9037A>G , LRG_293t1:c.9037A>G	NP_000050.2:p.Thr3013Ala
XM_011535203.1:c.9037A>G	XP_011533505.1:p.Thr3013Ala
XM_011535204.1:c.8941A>G	XP_011533506.1:p.Thr2981Ala
XM_011535205.1:c.*75A>G	XP_011533507.1:n.*75A>G
NM_000059.4:c.9037A>G MANE Select	NP_000050.3:p.Thr3013Ala