Canonical Allele Identifier: CA387767429

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137665407
• MyVariant Identifiers: chr13:g.32972616G>C (hg19) ; chr13:g.32398479G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398479G>C , CM000675.2:g.32398479G>C	GRCh38
NC_000013.10:g.32972616G>C , CM000675.1:g.32972616G>C	GRCh37
NC_000013.9:g.31870616G>C	NCBI36
NG_012772.3:g.88000G>C , LRG_293:g.88000G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*489G>C	ENSP00000434898.2:n.*489G>C
ENST00000528762.2:c.*1333G>C	ENSP00000433168.2:n.*1333G>C
ENST00000530893.7:c.9597G>C	ENSP00000499438.2:p.Met3199Ile
ENST00000665585.2:c.*1528G>C	ENSP00000499570.2:n.*1528G>C
ENST00000700202.2:c.9915G>C	ENSP00000514856.2:p.Met3305Ile
ENST00000700202.1:c.2382G>C	ENSP00000514856.1:p.Met794Ile
ENST00000700203.1:n.2093G>C
ENST00000380152.8:c.9966G>C MANE Select	ENSP00000369497.3:p.Met3322Ile
ENST00000544455.6:c.9966G>C	ENSP00000439902.1:p.Met3322Ile
ENST00000614259.2:c.9974G>C	ENSP00000506251.1:n.9974G>C
ENST00000680887.1:c.9966G>C	ENSP00000505508.1:p.Met3322Ile
ENST00000380152.7:c.9966G>C	ENSP00000369497.3:p.Met3322Ile
ENST00000544455.5:c.9966G>C	ENSP00000439902.1:p.Met3322Ile
NM_000059.3:c.9966G>C , LRG_293t1:c.9966G>C	NP_000050.2:p.Met3322Ile
XM_011535203.1:c.9966G>C	XP_011533505.1:p.Met3322Ile
XM_011535204.1:c.9870G>C	XP_011533506.1:p.Met3290Ile
NM_000059.4:c.9966G>C MANE Select	NP_000050.3:p.Met3322Ile