Canonical Allele Identifier: CA387766165

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137664025
• MyVariant Identifiers: chr13:g.32972461T>G (hg19) ; chr13:g.32398324T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398324T>G , CM000675.2:g.32398324T>G	GRCh38
NC_000013.10:g.32972461T>G , CM000675.1:g.32972461T>G	GRCh37
NC_000013.9:g.31870461T>G	NCBI36
NG_012772.3:g.87845T>G , LRG_293:g.87845T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*334T>G	ENSP00000434898.2:n.*334T>G
ENST00000528762.2:c.*1178T>G	ENSP00000433168.2:n.*1178T>G
ENST00000530893.7:c.9442T>G	ENSP00000499438.2:p.Leu3148Val
ENST00000665585.2:c.*1373T>G	ENSP00000499570.2:n.*1373T>G
ENST00000700202.2:c.9760T>G	ENSP00000514856.2:p.Leu3254Val
ENST00000700202.1:c.2227T>G	ENSP00000514856.1:p.Leu743Val
ENST00000700203.1:n.1938T>G
ENST00000380152.8:c.9811T>G MANE Select	ENSP00000369497.3:p.Leu3271Val
ENST00000544455.6:c.9811T>G	ENSP00000439902.1:p.Leu3271Val
ENST00000614259.2:c.9819T>G	ENSP00000506251.1:n.9819T>G
ENST00000680887.1:c.9811T>G	ENSP00000505508.1:p.Leu3271Val
ENST00000380152.7:c.9811T>G	ENSP00000369497.3:p.Leu3271Val
ENST00000533776.1:n.399T>G
ENST00000544455.5:c.9811T>G	ENSP00000439902.1:p.Leu3271Val
NM_000059.3:c.9811T>G , LRG_293t1:c.9811T>G	NP_000050.2:p.Leu3271Val
XM_011535203.1:c.9811T>G	XP_011533505.1:p.Leu3271Val
XM_011535204.1:c.9715T>G	XP_011533506.1:p.Leu3239Val
NM_000059.4:c.9811T>G MANE Select	NP_000050.3:p.Leu3271Val