Canonical Allele Identifier: CA387766650

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 655549
• ClinVar RCV Id: RCV000811745
• dbSNP Id: rs1593201942
• MyVariant Identifiers: chr13:g.32972521T>A (hg19) ; chr13:g.32398384T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398384T>A , CM000675.2:g.32398384T>A	GRCh38
NC_000013.10:g.32972521T>A , CM000675.1:g.32972521T>A	GRCh37
NC_000013.9:g.31870521T>A	NCBI36
NG_012772.3:g.87905T>A , LRG_293:g.87905T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*394T>A	ENSP00000434898.2:n.*394T>A
ENST00000528762.2:c.*1238T>A	ENSP00000433168.2:n.*1238T>A
ENST00000530893.7:c.9502T>A	ENSP00000499438.2:p.Ser3168Thr
ENST00000665585.2:c.*1433T>A	ENSP00000499570.2:n.*1433T>A
ENST00000700202.2:c.9820T>A	ENSP00000514856.2:p.Ser3274Thr
ENST00000700202.1:c.2287T>A	ENSP00000514856.1:p.Ser763Thr
ENST00000700203.1:n.1998T>A
ENST00000380152.8:c.9871T>A MANE Select	ENSP00000369497.3:p.Ser3291Thr
ENST00000544455.6:c.9871T>A	ENSP00000439902.1:p.Ser3291Thr
ENST00000614259.2:c.9879T>A	ENSP00000506251.1:n.9879T>A
ENST00000680887.1:c.9871T>A	ENSP00000505508.1:p.Ser3291Thr
ENST00000380152.7:c.9871T>A	ENSP00000369497.3:p.Ser3291Thr
ENST00000533776.1:n.459T>A
ENST00000544455.5:c.9871T>A	ENSP00000439902.1:p.Ser3291Thr
NM_000059.3:c.9871T>A , LRG_293t1:c.9871T>A	NP_000050.2:p.Ser3291Thr
XM_011535203.1:c.9871T>A	XP_011533505.1:p.Ser3291Thr
XM_011535204.1:c.9775T>A	XP_011533506.1:p.Ser3259Thr
NM_000059.4:c.9871T>A MANE Select	NP_000050.3:p.Ser3291Thr