Canonical Allele Identifier: CA387766439

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137664349
• MyVariant Identifiers: chr13:g.32972495C>A (hg19) ; chr13:g.32398358C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398358C>A , CM000675.2:g.32398358C>A	GRCh38
NC_000013.10:g.32972495C>A , CM000675.1:g.32972495C>A	GRCh37
NC_000013.9:g.31870495C>A	NCBI36
NG_012772.3:g.87879C>A , LRG_293:g.87879C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*368C>A	ENSP00000434898.2:n.*368C>A
ENST00000528762.2:c.*1212C>A	ENSP00000433168.2:n.*1212C>A
ENST00000530893.7:c.9476C>A	ENSP00000499438.2:p.Pro3159His
ENST00000665585.2:c.*1407C>A	ENSP00000499570.2:n.*1407C>A
ENST00000700202.2:c.9794C>A	ENSP00000514856.2:p.Pro3265His
ENST00000700202.1:c.2261C>A	ENSP00000514856.1:p.Pro754His
ENST00000700203.1:n.1972C>A
ENST00000380152.8:c.9845C>A MANE Select	ENSP00000369497.3:p.Pro3282His
ENST00000544455.6:c.9845C>A	ENSP00000439902.1:p.Pro3282His
ENST00000614259.2:c.9853C>A	ENSP00000506251.1:n.9853C>A
ENST00000680887.1:c.9845C>A	ENSP00000505508.1:p.Pro3282His
ENST00000380152.7:c.9845C>A	ENSP00000369497.3:p.Pro3282His
ENST00000533776.1:n.433C>A
ENST00000544455.5:c.9845C>A	ENSP00000439902.1:p.Pro3282His
NM_000059.3:c.9845C>A , LRG_293t1:c.9845C>A	NP_000050.2:p.Pro3282His
XM_011535203.1:c.9845C>A	XP_011533505.1:p.Pro3282His
XM_011535204.1:c.9749C>A	XP_011533506.1:p.Pro3250His
NM_000059.4:c.9845C>A MANE Select	NP_000050.3:p.Pro3282His