Canonical Allele Identifier: CA387767878

Gene: BRCA2

Linked Data

• dbSNP Id: rs1555290031
• MyVariant Identifiers: chr13:g.32972714G>C (hg19) ; chr13:g.32398577G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398577G>C , CM000675.2:g.32398577G>C	GRCh38
NC_000013.10:g.32972714G>C , CM000675.1:g.32972714G>C	GRCh37
NC_000013.9:g.31870714G>C	NCBI36
NG_012772.3:g.88098G>C , LRG_293:g.88098G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*587G>C	ENSP00000434898.2:n.*587G>C
ENST00000528762.2:c.*1431G>C	ENSP00000433168.2:n.*1431G>C
ENST00000530893.7:c.9695G>C	ENSP00000499438.2:p.Gly3232Ala
ENST00000665585.2:c.*1626G>C	ENSP00000499570.2:n.*1626G>C
ENST00000700202.2:c.10013G>C	ENSP00000514856.2:p.Gly3338Ala
ENST00000700202.1:c.2480G>C	ENSP00000514856.1:p.Gly827Ala
ENST00000700203.1:n.2191G>C
ENST00000380152.8:c.10064G>C MANE Select	ENSP00000369497.3:p.Gly3355Ala
ENST00000544455.6:c.10064G>C	ENSP00000439902.1:p.Gly3355Ala
ENST00000614259.2:c.10072G>C	ENSP00000506251.1:n.10072G>C
ENST00000680887.1:c.10064G>C	ENSP00000505508.1:p.Gly3355Ala
ENST00000380152.7:c.10064G>C	ENSP00000369497.3:p.Gly3355Ala
ENST00000544455.5:c.10064G>C	ENSP00000439902.1:p.Gly3355Ala
NM_000059.3:c.10064G>C , LRG_293t1:c.10064G>C	NP_000050.2:p.Gly3355Ala
XM_011535203.1:c.10064G>C	XP_011533505.1:p.Gly3355Ala
XM_011535204.1:c.9968G>C	XP_011533506.1:p.Gly3323Ala
NM_000059.4:c.10064G>C MANE Select	NP_000050.3:p.Gly3355Ala