Canonical Allele Identifier: CA387766563

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137664460
• gnomAD v4: 13-32398372-T-C
• MyVariant Identifiers: chr13:g.32972509T>C (hg19) ; chr13:g.32398372T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398372T>C , CM000675.2:g.32398372T>C	GRCh38
NC_000013.10:g.32972509T>C , CM000675.1:g.32972509T>C	GRCh37
NC_000013.9:g.31870509T>C	NCBI36
NG_012772.3:g.87893T>C , LRG_293:g.87893T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*382T>C	ENSP00000434898.2:n.*382T>C
ENST00000528762.2:c.*1226T>C	ENSP00000433168.2:n.*1226T>C
ENST00000530893.7:c.9490T>C	ENSP00000499438.2:p.Cys3164Arg
ENST00000665585.2:c.*1421T>C	ENSP00000499570.2:n.*1421T>C
ENST00000700202.2:c.9808T>C	ENSP00000514856.2:p.Cys3270Arg
ENST00000700202.1:c.2275T>C	ENSP00000514856.1:p.Cys759Arg
ENST00000700203.1:n.1986T>C
ENST00000380152.8:c.9859T>C MANE Select	ENSP00000369497.3:p.Cys3287Arg
ENST00000544455.6:c.9859T>C	ENSP00000439902.1:p.Cys3287Arg
ENST00000614259.2:c.9867T>C	ENSP00000506251.1:n.9867T>C
ENST00000680887.1:c.9859T>C	ENSP00000505508.1:p.Cys3287Arg
ENST00000380152.7:c.9859T>C	ENSP00000369497.3:p.Cys3287Arg
ENST00000533776.1:n.447T>C
ENST00000544455.5:c.9859T>C	ENSP00000439902.1:p.Cys3287Arg
NM_000059.3:c.9859T>C , LRG_293t1:c.9859T>C	NP_000050.2:p.Cys3287Arg
XM_011535203.1:c.9859T>C	XP_011533505.1:p.Cys3287Arg
XM_011535204.1:c.9763T>C	XP_011533506.1:p.Cys3255Arg
NM_000059.4:c.9859T>C MANE Select	NP_000050.3:p.Cys3287Arg