Canonical Allele Identifier: CA483438904

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 2004179
• ClinVar RCV Id: RCV002815917
• dbSNP Id: rs2137520664
• MyVariant Identifiers: chr13:g.32914252T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32340115T>A , CM000675.2:g.32340115T>A	GRCh38
NC_000013.10:g.32914252T>A , CM000675.1:g.32914252T>A	GRCh37
NC_000013.9:g.31812252T>A	NCBI36
NG_012772.3:g.29636T>A , LRG_293:g.29636T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.5760T>A	ENSP00000434898.2:p.Val1920=
ENST00000528762.2:c.5760T>A	ENSP00000433168.2:p.Val1920=
ENST00000530893.7:c.5391T>A	ENSP00000499438.2:p.Val1797=
ENST00000665585.2:c.5760T>A	ENSP00000499570.2:p.Val1920=
ENST00000666593.2:c.5760T>A	ENSP00000499256.2:p.Val1920=
ENST00000700202.2:c.5760T>A	ENSP00000514856.2:p.Val1920=
ENST00000380152.8:c.5760T>A MANE Select	ENSP00000369497.3:p.Val1920=
ENST00000544455.6:c.5760T>A	ENSP00000439902.1:p.Val1920=
ENST00000614259.2:c.5760T>A	ENSP00000506251.1:p.Val1920=
ENST00000680887.1:c.5760T>A	ENSP00000505508.1:p.Val1920=
ENST00000380152.7:c.5760T>A	ENSP00000369497.3:p.Val1920=
ENST00000544455.5:c.5760T>A	ENSP00000439902.1:p.Val1920=
ENST00000614259.1:n.5760T>A
NM_000059.3:c.5760T>A , LRG_293t1:c.5760T>A	NP_000050.2:p.Val1920=
XM_011535203.1:c.5760T>A	XP_011533505.1:p.Val1920=
XM_011535204.1:c.5760T>A	XP_011533506.1:p.Val1920=
XM_011535205.1:c.5760T>A	XP_011533507.1:p.Val1920=
NM_000059.4:c.5760T>A MANE Select	NP_000050.3:p.Val1920=