Canonical Allele Identifier: CA025304

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 52424
• ClinVar RCV Id: RCV000045327 ; RCV000113832 ; RCV000165314 ; RCV001762151
• dbSNP Id: rs80359010
• gnomAD v2: 13-32936686-A-G
• gnomAD v4: 13-32362549-A-G
• MyVariant Identifiers: chr13:g.32936686A>G (hg19) ; chr13:g.32362549A>G (hg38)
• PubMed: PMID:10923033 ; PMID:16030099 ; PMID:17899372 ; PMID:19043619

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362549A>G , CM000675.2:g.32362549A>G	GRCh38
NC_000013.10:g.32936686A>G , CM000675.1:g.32936686A>G	GRCh37
NC_000013.9:g.31834686A>G	NCBI36
NG_012772.3:g.52070A>G , LRG_293:g.52070A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7832A>G	ENSP00000434898.2:p.Asp2611Gly
ENST00000528762.2:c.7832A>G	ENSP00000433168.2:p.Asp2611Gly
ENST00000530893.7:c.7463A>G	ENSP00000499438.2:p.Asp2488Gly
ENST00000665585.2:c.7832A>G	ENSP00000499570.2:p.Asp2611Gly
ENST00000666593.2:c.7832A>G	ENSP00000499256.2:p.Asp2611Gly
ENST00000700202.2:c.7832A>G	ENSP00000514856.2:p.Asp2611Gly
ENST00000700202.1:c.299A>G	ENSP00000514856.1:p.Asp100Gly
ENST00000380152.8:c.7832A>G MANE Select	ENSP00000369497.3:p.Asp2611Gly
ENST00000544455.6:c.7832A>G	ENSP00000439902.1:p.Asp2611Gly
ENST00000614259.2:c.7840A>G	ENSP00000506251.1:p.Ile2614Val
ENST00000665585.1:c.397A>G
ENST00000680887.1:c.7832A>G	ENSP00000505508.1:p.Asp2611Gly
ENST00000380152.7:c.7832A>G	ENSP00000369497.3:p.Asp2611Gly
ENST00000544455.5:c.7832A>G	ENSP00000439902.1:p.Asp2611Gly
ENST00000614259.1:n.7840A>G
NM_000059.3:c.7832A>G , LRG_293t1:c.7832A>G	NP_000050.2:p.Asp2611Gly
XM_011535203.1:c.7832A>G	XP_011533505.1:p.Asp2611Gly
XM_011535204.1:c.7736A>G	XP_011533506.1:p.Asp2579Gly
XM_011535205.1:c.7832A>G	XP_011533507.1:p.Asp2611Gly
NM_000059.4:c.7832A>G MANE Select	NP_000050.3:p.Asp2611Gly