Canonical Allele Identifier: CA387766243

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137664088
• MyVariant Identifiers: chr13:g.32972469C>G (hg19) ; chr13:g.32398332C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398332C>G , CM000675.2:g.32398332C>G	GRCh38
NC_000013.10:g.32972469C>G , CM000675.1:g.32972469C>G	GRCh37
NC_000013.9:g.31870469C>G	NCBI36
NG_012772.3:g.87853C>G , LRG_293:g.87853C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*342C>G	ENSP00000434898.2:n.*342C>G
ENST00000528762.2:c.*1186C>G	ENSP00000433168.2:n.*1186C>G
ENST00000530893.7:c.9450C>G	ENSP00000499438.2:p.Phe3150Leu
ENST00000665585.2:c.*1381C>G	ENSP00000499570.2:n.*1381C>G
ENST00000700202.2:c.9768C>G	ENSP00000514856.2:p.Phe3256Leu
ENST00000700202.1:c.2235C>G	ENSP00000514856.1:p.Phe745Leu
ENST00000700203.1:n.1946C>G
ENST00000380152.8:c.9819C>G MANE Select	ENSP00000369497.3:p.Phe3273Leu
ENST00000544455.6:c.9819C>G	ENSP00000439902.1:p.Phe3273Leu
ENST00000614259.2:c.9827C>G	ENSP00000506251.1:n.9827C>G
ENST00000680887.1:c.9819C>G	ENSP00000505508.1:p.Phe3273Leu
ENST00000380152.7:c.9819C>G	ENSP00000369497.3:p.Phe3273Leu
ENST00000533776.1:n.407C>G
ENST00000544455.5:c.9819C>G	ENSP00000439902.1:p.Phe3273Leu
NM_000059.3:c.9819C>G , LRG_293t1:c.9819C>G	NP_000050.2:p.Phe3273Leu
XM_011535203.1:c.9819C>G	XP_011533505.1:p.Phe3273Leu
XM_011535204.1:c.9723C>G	XP_011533506.1:p.Phe3241Leu
NM_000059.4:c.9819C>G MANE Select	NP_000050.3:p.Phe3273Leu