Canonical Allele Identifier: CA387757586

Gene: BRCA2

Linked Data

• dbSNP Id: rs587781493
• MyVariant Identifiers: chr13:g.32954004A>T (hg19) ; chr13:g.32379867A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379867A>T , CM000675.2:g.32379867A>T	GRCh38
NC_000013.10:g.32954004A>T , CM000675.1:g.32954004A>T	GRCh37
NC_000013.9:g.31852004A>T	NCBI36
NG_012772.3:g.69388A>T , LRG_293:g.69388A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.9071A>T	ENSP00000434898.2:p.Asn3024Ile
ENST00000528762.2:c.*438A>T	ENSP00000433168.2:n.*438A>T
ENST00000530893.7:c.8702A>T	ENSP00000499438.2:p.Asn2901Ile
ENST00000665585.2:c.*633A>T	ENSP00000499570.2:n.*633A>T
ENST00000666593.2:c.9071A>T	ENSP00000499256.2:p.Asn3024Ile
ENST00000700202.2:c.9020A>T	ENSP00000514856.2:p.Asn3007Ile
ENST00000700202.1:c.1487A>T	ENSP00000514856.1:p.Asn496Ile
ENST00000700203.1:n.1198A>T
ENST00000380152.8:c.9071A>T MANE Select	ENSP00000369497.3:p.Asn3024Ile
ENST00000544455.6:c.9071A>T	ENSP00000439902.1:p.Asn3024Ile
ENST00000614259.2:c.9079A>T	ENSP00000506251.1:n.9079A>T
ENST00000665585.1:c.1949A>T
ENST00000680887.1:c.9071A>T	ENSP00000505508.1:p.Asn3024Ile
ENST00000380152.7:c.9071A>T	ENSP00000369497.3:p.Asn3024Ile
ENST00000470094.1:c.28A>T
ENST00000544455.5:c.9071A>T	ENSP00000439902.1:p.Asn3024Ile
NM_000059.3:c.9071A>T , LRG_293t1:c.9071A>T	NP_000050.2:p.Asn3024Ile
XM_011535203.1:c.9071A>T	XP_011533505.1:p.Asn3024Ile
XM_011535204.1:c.8975A>T	XP_011533506.1:p.Asn2992Ile
NM_000059.4:c.9071A>T MANE Select	NP_000050.3:p.Asn3024Ile