Canonical Allele Identifier: CA483440190

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137664438
• MyVariant Identifiers: chr13:g.32972505C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398368C>A , CM000675.2:g.32398368C>A	GRCh38
NC_000013.10:g.32972505C>A , CM000675.1:g.32972505C>A	GRCh37
NC_000013.9:g.31870505C>A	NCBI36
NG_012772.3:g.87889C>A , LRG_293:g.87889C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*378C>A	ENSP00000434898.2:n.*378C>A
ENST00000528762.2:c.*1222C>A	ENSP00000433168.2:n.*1222C>A
ENST00000530893.7:c.9486C>A	ENSP00000499438.2:p.Pro3162=
ENST00000665585.2:c.*1417C>A	ENSP00000499570.2:n.*1417C>A
ENST00000700202.2:c.9804C>A	ENSP00000514856.2:p.Pro3268=
ENST00000700202.1:c.2271C>A	ENSP00000514856.1:p.Pro757=
ENST00000700203.1:n.1982C>A
ENST00000380152.8:c.9855C>A MANE Select	ENSP00000369497.3:p.Pro3285=
ENST00000544455.6:c.9855C>A	ENSP00000439902.1:p.Pro3285=
ENST00000614259.2:c.9863C>A	ENSP00000506251.1:n.9863C>A
ENST00000680887.1:c.9855C>A	ENSP00000505508.1:p.Pro3285=
ENST00000380152.7:c.9855C>A	ENSP00000369497.3:p.Pro3285=
ENST00000533776.1:n.443C>A
ENST00000544455.5:c.9855C>A	ENSP00000439902.1:p.Pro3285=
NM_000059.3:c.9855C>A , LRG_293t1:c.9855C>A	NP_000050.2:p.Pro3285=
XM_011535203.1:c.9855C>A	XP_011533505.1:p.Pro3285=
XM_011535204.1:c.9759C>A	XP_011533506.1:p.Pro3253=
NM_000059.4:c.9855C>A MANE Select	NP_000050.3:p.Pro3285=