Canonical Allele Identifier: CA247493382

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 2088785
• ClinVar RCV Id: RCV003011813
• dbSNP Id: rs1051853391
• MyVariant Identifiers: chr13:g.32953595G>A (hg19) ; chr13:g.32379458G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379458G>A , CM000675.2:g.32379458G>A	GRCh38
NC_000013.10:g.32953595G>A , CM000675.1:g.32953595G>A	GRCh37
NC_000013.9:g.31851595G>A	NCBI36
NG_012772.3:g.68979G>A , LRG_293:g.68979G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8896G>A	ENSP00000434898.2:p.Val2966Ile
ENST00000528762.2:c.*263G>A	ENSP00000433168.2:n.*263G>A
ENST00000530893.7:c.8527G>A	ENSP00000499438.2:p.Val2843Ile
ENST00000665585.2:c.*458G>A	ENSP00000499570.2:n.*458G>A
ENST00000666593.2:c.8896G>A	ENSP00000499256.2:p.Val2966Ile
ENST00000700202.2:c.8896G>A	ENSP00000514856.2:p.Val2966Ile
ENST00000700202.1:c.1363G>A	ENSP00000514856.1:p.Val455Ile
ENST00000700203.1:n.1023G>A
ENST00000380152.8:c.8896G>A MANE Select	ENSP00000369497.3:p.Val2966Ile
ENST00000544455.6:c.8896G>A	ENSP00000439902.1:p.Val2966Ile
ENST00000614259.2:c.8904G>A	ENSP00000506251.1:n.8904G>A
ENST00000665585.1:c.1774G>A
ENST00000680887.1:c.8896G>A	ENSP00000505508.1:p.Val2966Ile
ENST00000380152.7:c.8896G>A	ENSP00000369497.3:p.Val2966Ile
ENST00000528762.1:c.458G>A	ENSP00000433168.1:n.458G>A
ENST00000544455.5:c.8896G>A	ENSP00000439902.1:p.Val2966Ile
NM_000059.3:c.8896G>A , LRG_293t1:c.8896G>A	NP_000050.2:p.Val2966Ile
XM_011535203.1:c.8896G>A	XP_011533505.1:p.Val2966Ile
XM_011535204.1:c.8800G>A	XP_011533506.1:p.Val2934Ile
XM_011535205.1:c.8755-292G>A	XP_011533507.1:n.8755-292G>A
NM_000059.4:c.8896G>A MANE Select	NP_000050.3:p.Val2966Ile