Canonical Allele Identifier: CA387768114

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 462220
• ClinVar RCV Id: RCV000538319
• dbSNP Id: rs1412762465
• MyVariant Identifiers: chr13:g.32972786A>G (hg19) ; chr13:g.32398649A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398649A>G , CM000675.2:g.32398649A>G	GRCh38
NC_000013.10:g.32972786A>G , CM000675.1:g.32972786A>G	GRCh37
NC_000013.9:g.31870786A>G	NCBI36
NG_012772.3:g.88170A>G , LRG_293:g.88170A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*659A>G	ENSP00000434898.2:n.*659A>G
ENST00000528762.2:c.*1503A>G	ENSP00000433168.2:n.*1503A>G
ENST00000530893.7:c.9767A>G	ENSP00000499438.2:p.Tyr3256Cys
ENST00000665585.2:c.*1698A>G	ENSP00000499570.2:n.*1698A>G
ENST00000700202.2:c.10085A>G	ENSP00000514856.2:p.Tyr3362Cys
ENST00000700202.1:c.2552A>G	ENSP00000514856.1:p.Tyr851Cys
ENST00000700203.1:n.2263A>G
ENST00000380152.8:c.10136A>G MANE Select	ENSP00000369497.3:p.Tyr3379Cys
ENST00000544455.6:c.10136A>G	ENSP00000439902.1:p.Tyr3379Cys
ENST00000614259.2:c.10144A>G	ENSP00000506251.1:n.10144A>G
ENST00000680887.1:c.10136A>G	ENSP00000505508.1:p.Tyr3379Cys
ENST00000380152.7:c.10136A>G	ENSP00000369497.3:p.Tyr3379Cys
ENST00000544455.5:c.10136A>G	ENSP00000439902.1:p.Tyr3379Cys
NM_000059.3:c.10136A>G , LRG_293t1:c.10136A>G	NP_000050.2:p.Tyr3379Cys
XM_011535203.1:c.10136A>G	XP_011533505.1:p.Tyr3379Cys
XM_011535204.1:c.10040A>G	XP_011533506.1:p.Tyr3347Cys
NM_000059.4:c.10136A>G MANE Select	NP_000050.3:p.Tyr3379Cys