Canonical Allele Identifier: CA387766473

Gene: BRCA2

Linked Data

• dbSNP Id: rs1593201909
• MyVariant Identifiers: chr13:g.32972500A>T (hg19) ; chr13:g.32398363A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398363A>T , CM000675.2:g.32398363A>T	GRCh38
NC_000013.10:g.32972500A>T , CM000675.1:g.32972500A>T	GRCh37
NC_000013.9:g.31870500A>T	NCBI36
NG_012772.3:g.87884A>T , LRG_293:g.87884A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*373A>T	ENSP00000434898.2:n.*373A>T
ENST00000528762.2:c.*1217A>T	ENSP00000433168.2:n.*1217A>T
ENST00000530893.7:c.9481A>T	ENSP00000499438.2:p.Ser3161Cys
ENST00000665585.2:c.*1412A>T	ENSP00000499570.2:n.*1412A>T
ENST00000700202.2:c.9799A>T	ENSP00000514856.2:p.Ser3267Cys
ENST00000700202.1:c.2266A>T	ENSP00000514856.1:p.Ser756Cys
ENST00000700203.1:n.1977A>T
ENST00000380152.8:c.9850A>T MANE Select	ENSP00000369497.3:p.Ser3284Cys
ENST00000544455.6:c.9850A>T	ENSP00000439902.1:p.Ser3284Cys
ENST00000614259.2:c.9858A>T	ENSP00000506251.1:n.9858A>T
ENST00000680887.1:c.9850A>T	ENSP00000505508.1:p.Ser3284Cys
ENST00000380152.7:c.9850A>T	ENSP00000369497.3:p.Ser3284Cys
ENST00000533776.1:n.438A>T
ENST00000544455.5:c.9850A>T	ENSP00000439902.1:p.Ser3284Cys
NM_000059.3:c.9850A>T , LRG_293t1:c.9850A>T	NP_000050.2:p.Ser3284Cys
XM_011535203.1:c.9850A>T	XP_011533505.1:p.Ser3284Cys
XM_011535204.1:c.9754A>T	XP_011533506.1:p.Ser3252Cys
NM_000059.4:c.9850A>T MANE Select	NP_000050.3:p.Ser3284Cys