Canonical Allele Identifier: CA483438690

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137517075
• MyVariant Identifiers: chr13:g.32913883A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32339746A>T , CM000675.2:g.32339746A>T	GRCh38
NC_000013.10:g.32913883A>T , CM000675.1:g.32913883A>T	GRCh37
NC_000013.9:g.31811883A>T	NCBI36
NG_012772.3:g.29267A>T , LRG_293:g.29267A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.5391A>T	ENSP00000434898.2:p.Ala1797=
ENST00000528762.2:c.5391A>T	ENSP00000433168.2:p.Ala1797=
ENST00000530893.7:c.5022A>T	ENSP00000499438.2:p.Ala1674=
ENST00000665585.2:c.5391A>T	ENSP00000499570.2:p.Ala1797=
ENST00000666593.2:c.5391A>T	ENSP00000499256.2:p.Ala1797=
ENST00000700202.2:c.5391A>T	ENSP00000514856.2:p.Ala1797=
ENST00000380152.8:c.5391A>T MANE Select	ENSP00000369497.3:p.Ala1797=
ENST00000544455.6:c.5391A>T	ENSP00000439902.1:p.Ala1797=
ENST00000614259.2:c.5391A>T	ENSP00000506251.1:p.Ala1797=
ENST00000680887.1:c.5391A>T	ENSP00000505508.1:p.Ala1797=
ENST00000380152.7:c.5391A>T	ENSP00000369497.3:p.Ala1797=
ENST00000544455.5:c.5391A>T	ENSP00000439902.1:p.Ala1797=
ENST00000614259.1:n.5391A>T
NM_000059.3:c.5391A>T , LRG_293t1:c.5391A>T	NP_000050.2:p.Ala1797=
XM_011535203.1:c.5391A>T	XP_011533505.1:p.Ala1797=
XM_011535204.1:c.5391A>T	XP_011533506.1:p.Ala1797=
XM_011535205.1:c.5391A>T	XP_011533507.1:p.Ala1797=
NM_000059.4:c.5391A>T MANE Select	NP_000050.3:p.Ala1797=