Canonical Allele Identifier: CA387767825

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 3224978
• ClinVar RCV Id: RCV004521668
• dbSNP Id: rs2137666093
• MyVariant Identifiers: chr13:g.32972698C>A (hg19) ; chr13:g.32398561C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398561C>A , CM000675.2:g.32398561C>A	GRCh38
NC_000013.10:g.32972698C>A , CM000675.1:g.32972698C>A	GRCh37
NC_000013.9:g.31870698C>A	NCBI36
NG_012772.3:g.88082C>A , LRG_293:g.88082C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*571C>A	ENSP00000434898.2:n.*571C>A
ENST00000528762.2:c.*1415C>A	ENSP00000433168.2:n.*1415C>A
ENST00000530893.7:c.9679C>A	ENSP00000499438.2:p.Gln3227Lys
ENST00000665585.2:c.*1610C>A	ENSP00000499570.2:n.*1610C>A
ENST00000700202.2:c.9997C>A	ENSP00000514856.2:p.Gln3333Lys
ENST00000700202.1:c.2464C>A	ENSP00000514856.1:p.Gln822Lys
ENST00000700203.1:n.2175C>A
ENST00000380152.8:c.10048C>A MANE Select	ENSP00000369497.3:p.Gln3350Lys
ENST00000544455.6:c.10048C>A	ENSP00000439902.1:p.Gln3350Lys
ENST00000614259.2:c.10056C>A	ENSP00000506251.1:n.10056C>A
ENST00000680887.1:c.10048C>A	ENSP00000505508.1:p.Gln3350Lys
ENST00000380152.7:c.10048C>A	ENSP00000369497.3:p.Gln3350Lys
ENST00000544455.5:c.10048C>A	ENSP00000439902.1:p.Gln3350Lys
NM_000059.3:c.10048C>A , LRG_293t1:c.10048C>A	NP_000050.2:p.Gln3350Lys
XM_011535203.1:c.10048C>A	XP_011533505.1:p.Gln3350Lys
XM_011535204.1:c.9952C>A	XP_011533506.1:p.Gln3318Lys
NM_000059.4:c.10048C>A MANE Select	NP_000050.3:p.Gln3350Lys