Canonical Allele Identifier: CA387793158

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 567495
• ClinVar RCV Id: RCV000687596 ; RCV002360725
• dbSNP Id: rs587781842
• MyVariant Identifiers: chr13:g.32921023G>C (hg19) ; chr13:g.32346886G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32346886G>C , CM000675.2:g.32346886G>C	GRCh38
NC_000013.10:g.32921023G>C , CM000675.1:g.32921023G>C	GRCh37
NC_000013.9:g.31819023G>C	NCBI36
NG_012772.3:g.36407G>C , LRG_293:g.36407G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.6997G>C	ENSP00000434898.2:p.Val2333Leu
ENST00000528762.2:c.6997G>C	ENSP00000433168.2:p.Val2333Leu
ENST00000530893.7:c.6628G>C	ENSP00000499438.2:p.Val2210Leu
ENST00000665585.2:c.6997G>C	ENSP00000499570.2:p.Val2333Leu
ENST00000666593.2:c.6997G>C	ENSP00000499256.2:p.Val2333Leu
ENST00000700202.2:c.6997G>C	ENSP00000514856.2:p.Val2333Leu
ENST00000380152.8:c.6997G>C MANE Select	ENSP00000369497.3:p.Val2333Leu
ENST00000544455.6:c.6997G>C	ENSP00000439902.1:p.Val2333Leu
ENST00000614259.2:c.6997G>C	ENSP00000506251.1:p.Val2333Leu
ENST00000680887.1:c.6997G>C	ENSP00000505508.1:p.Val2333Leu
ENST00000380152.7:c.6997G>C	ENSP00000369497.3:p.Val2333Leu
ENST00000544455.5:c.6997G>C	ENSP00000439902.1:p.Val2333Leu
ENST00000614259.1:n.6997G>C
NM_000059.3:c.6997G>C , LRG_293t1:c.6997G>C	NP_000050.2:p.Val2333Leu
XM_011535203.1:c.6997G>C	XP_011533505.1:p.Val2333Leu
XM_011535204.1:c.6901G>C	XP_011533506.1:p.Val2301Leu
XM_011535205.1:c.6997G>C	XP_011533507.1:p.Val2333Leu
NM_000059.4:c.6997G>C MANE Select	NP_000050.3:p.Val2333Leu