Canonical Allele Identifier: CA658683808

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 491232
• ClinVar RCV Id: RCV000581999 ; RCV003645063
• dbSNP Id: rs1555280441
• MyVariant Identifiers: chr13:g.32893469A>T (hg19) ; chr13:g.32319332A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32319332A>T , CM000675.2:g.32319332A>T	GRCh38
NC_000013.10:g.32893469A>T , CM000675.1:g.32893469A>T	GRCh37
NC_000013.9:g.31791469A>T	NCBI36
NG_012772.3:g.8853A>T , LRG_293:g.8853A>T
NG_017006.2:g.1032T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.316+7A>T	ENSP00000434898.2:n.316+7A>T
ENST00000528762.2:c.316+7A>T	ENSP00000433168.2:n.316+7A>T
ENST00000530893.7:c.-54+7A>T	ENSP00000499438.2:n.-54+7A>T
ENST00000665585.2:c.316+7A>T	ENSP00000499570.2:n.316+7A>T
ENST00000666593.2:c.316+7A>T	ENSP00000499256.2:n.316+7A>T
ENST00000700202.2:c.316+7A>T	ENSP00000514856.2:n.316+7A>T
ENST00000700200.1:n.191+2805A>T
ENST00000700201.1:c.316+7A>T	ENSP00000514855.1:n.316+7A>T
ENST00000380152.8:c.316+7A>T MANE Select	ENSP00000369497.3:n.316+7A>T
ENST00000544455.6:c.316+7A>T	ENSP00000439902.1:n.316+7A>T
ENST00000614259.2:c.316+7A>T	ENSP00000506251.1:n.316+7A>T
ENST00000680887.1:c.316+7A>T	ENSP00000505508.1:n.316+7A>T
ENST00000380152.7:c.316+7A>T	ENSP00000369497.3:n.316+7A>T
ENST00000530893.6:n.514+7A>T
ENST00000544455.5:c.316+7A>T	ENSP00000439902.1:n.316+7A>T
ENST00000614259.1:n.316+7A>T
NM_000059.3:c.316+7A>T , LRG_293t1:c.316+7A>T	NP_000050.2:n.316+7A>T
XM_011535203.1:c.316+7A>T	XP_011533505.1:n.316+7A>T
XM_011535204.1:c.316+7A>T	XP_011533506.1:n.316+7A>T
XM_011535205.1:c.316+7A>T	XP_011533507.1:n.316+7A>T
NM_000059.4:c.316+7A>T MANE Select	NP_000050.3:n.316+7A>T