Canonical Allele Identifier: CA387756495

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 633105
• ClinVar RCV Id: RCV000781054 ; RCV001856192
• dbSNP Id: rs1555288392
• gnomAD v4: 13-32379453-G-C
• MyVariant Identifiers: chr13:g.32953590G>C (hg19) ; chr13:g.32379453G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379453G>C , CM000675.2:g.32379453G>C	GRCh38
NC_000013.10:g.32953590G>C , CM000675.1:g.32953590G>C	GRCh37
NC_000013.9:g.31851590G>C	NCBI36
NG_012772.3:g.68974G>C , LRG_293:g.68974G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8891G>C	ENSP00000434898.2:p.Arg2964Thr
ENST00000528762.2:c.*258G>C	ENSP00000433168.2:n.*258G>C
ENST00000530893.7:c.8522G>C	ENSP00000499438.2:p.Arg2841Thr
ENST00000665585.2:c.*453G>C	ENSP00000499570.2:n.*453G>C
ENST00000666593.2:c.8891G>C	ENSP00000499256.2:p.Arg2964Thr
ENST00000700202.2:c.8891G>C	ENSP00000514856.2:p.Arg2964Thr
ENST00000700202.1:c.1358G>C	ENSP00000514856.1:p.Arg453Thr
ENST00000700203.1:n.1018G>C
ENST00000380152.8:c.8891G>C MANE Select	ENSP00000369497.3:p.Arg2964Thr
ENST00000544455.6:c.8891G>C	ENSP00000439902.1:p.Arg2964Thr
ENST00000614259.2:c.8899G>C	ENSP00000506251.1:n.8899G>C
ENST00000665585.1:c.1769G>C
ENST00000680887.1:c.8891G>C	ENSP00000505508.1:p.Arg2964Thr
ENST00000380152.7:c.8891G>C	ENSP00000369497.3:p.Arg2964Thr
ENST00000528762.1:c.453G>C	ENSP00000433168.1:n.453G>C
ENST00000544455.5:c.8891G>C	ENSP00000439902.1:p.Arg2964Thr
NM_000059.3:c.8891G>C , LRG_293t1:c.8891G>C	NP_000050.2:p.Arg2964Thr
XM_011535203.1:c.8891G>C	XP_011533505.1:p.Arg2964Thr
XM_011535204.1:c.8795G>C	XP_011533506.1:p.Arg2932Thr
XM_011535205.1:c.8755-297G>C	XP_011533507.1:n.8755-297G>C
NM_000059.4:c.8891G>C MANE Select	NP_000050.3:p.Arg2964Thr