Canonical Allele Identifier: CA387756378

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 802952
• ClinVar RCV Id: RCV000989078 ; RCV002549721
• dbSNP Id: rs276174913
• gnomAD v4: 13-32379431-C-A
• MyVariant Identifiers: chr13:g.32953568C>A (hg19) ; chr13:g.32379431C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379431C>A , CM000675.2:g.32379431C>A	GRCh38
NC_000013.10:g.32953568C>A , CM000675.1:g.32953568C>A	GRCh37
NC_000013.9:g.31851568C>A	NCBI36
NG_012772.3:g.68952C>A , LRG_293:g.68952C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8869C>A	ENSP00000434898.2:p.Gln2957Lys
ENST00000528762.2:c.*236C>A	ENSP00000433168.2:n.*236C>A
ENST00000530893.7:c.8500C>A	ENSP00000499438.2:p.Gln2834Lys
ENST00000665585.2:c.*431C>A	ENSP00000499570.2:n.*431C>A
ENST00000666593.2:c.8869C>A	ENSP00000499256.2:p.Gln2957Lys
ENST00000700202.2:c.8869C>A	ENSP00000514856.2:p.Gln2957Lys
ENST00000700202.1:c.1336C>A	ENSP00000514856.1:p.Gln446Lys
ENST00000700203.1:n.996C>A
ENST00000380152.8:c.8869C>A MANE Select	ENSP00000369497.3:p.Gln2957Lys
ENST00000544455.6:c.8869C>A	ENSP00000439902.1:p.Gln2957Lys
ENST00000614259.2:c.8877C>A	ENSP00000506251.1:n.8877C>A
ENST00000665585.1:c.1747C>A
ENST00000680887.1:c.8869C>A	ENSP00000505508.1:p.Gln2957Lys
ENST00000380152.7:c.8869C>A	ENSP00000369497.3:p.Gln2957Lys
ENST00000528762.1:c.431C>A	ENSP00000433168.1:n.431C>A
ENST00000544455.5:c.8869C>A	ENSP00000439902.1:p.Gln2957Lys
NM_000059.3:c.8869C>A , LRG_293t1:c.8869C>A	NP_000050.2:p.Gln2957Lys
XM_011535203.1:c.8869C>A	XP_011533505.1:p.Gln2957Lys
XM_011535204.1:c.8773C>A	XP_011533506.1:p.Gln2925Lys
XM_011535205.1:c.8755-319C>A	XP_011533507.1:n.8755-319C>A
NM_000059.4:c.8869C>A MANE Select	NP_000050.3:p.Gln2957Lys