Canonical Allele Identifier: CA387765388

Gene: BRCA2

Linked Data

• dbSNP Id: rs1566260847
• MyVariant Identifiers: chr13:g.32972352G>T (hg19) ; chr13:g.32398215G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398215G>T , CM000675.2:g.32398215G>T	GRCh38
NC_000013.10:g.32972352G>T , CM000675.1:g.32972352G>T	GRCh37
NC_000013.9:g.31870352G>T	NCBI36
NG_012772.3:g.87736G>T , LRG_293:g.87736G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*225G>T	ENSP00000434898.2:n.*225G>T
ENST00000528762.2:c.*1069G>T	ENSP00000433168.2:n.*1069G>T
ENST00000530893.7:c.9333G>T	ENSP00000499438.2:p.Met3111Ile
ENST00000665585.2:c.*1264G>T	ENSP00000499570.2:n.*1264G>T
ENST00000700202.2:c.9651G>T	ENSP00000514856.2:p.Met3217Ile
ENST00000700202.1:c.2118G>T	ENSP00000514856.1:p.Met706Ile
ENST00000700203.1:n.1829G>T
ENST00000380152.8:c.9702G>T MANE Select	ENSP00000369497.3:p.Met3234Ile
ENST00000544455.6:c.9702G>T	ENSP00000439902.1:p.Met3234Ile
ENST00000614259.2:c.9710G>T	ENSP00000506251.1:n.9710G>T
ENST00000665585.1:c.2580G>T
ENST00000680887.1:c.9702G>T	ENSP00000505508.1:p.Met3234Ile
ENST00000380152.7:c.9702G>T	ENSP00000369497.3:p.Met3234Ile
ENST00000470094.1:c.785G>T
ENST00000533776.1:n.290G>T
ENST00000544455.5:c.9702G>T	ENSP00000439902.1:p.Met3234Ile
NM_000059.3:c.9702G>T , LRG_293t1:c.9702G>T	NP_000050.2:p.Met3234Ile
XM_011535203.1:c.9702G>T	XP_011533505.1:p.Met3234Ile
XM_011535204.1:c.9606G>T	XP_011533506.1:p.Met3202Ile
NM_000059.4:c.9702G>T MANE Select	NP_000050.3:p.Met3234Ile