Canonical Allele Identifier: CA026098

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 38230
• ClinVar RCV Id: RCV000031813 ; RCV000045787 ; RCV000162632 ; RCV000657062 ; RCV001798057 ; RCV003473230
• dbSNP Id: rs28897758
• gnomAD v3: 13-32394734-T-G
• gnomAD v4: 13-32394734-T-G
• MyVariant Identifiers: chr13:g.32968871T>G (hg19) ; chr13:g.32394734T>G (hg38)
• PubMed: PMID:10923033 ; PMID:18724707 ; PMID:19043619 ; PMID:25859162

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32394734T>G , CM000675.2:g.32394734T>G	GRCh38
NC_000013.10:g.32968871T>G , CM000675.1:g.32968871T>G	GRCh37
NC_000013.9:g.31866871T>G	NCBI36
NG_012772.3:g.84255T>G , LRG_293:g.84255T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.9302T>G	ENSP00000434898.2:p.Leu3101Arg
ENST00000528762.2:c.*669T>G	ENSP00000433168.2:n.*669T>G
ENST00000530893.7:c.8933T>G	ENSP00000499438.2:p.Leu2978Arg
ENST00000665585.2:c.*864T>G	ENSP00000499570.2:n.*864T>G
ENST00000666593.2:c.*147T>G	ENSP00000499256.2:n.*147T>G
ENST00000700202.2:c.9251T>G	ENSP00000514856.2:p.Leu3084Arg
ENST00000700202.1:c.1718T>G	ENSP00000514856.1:p.Leu573Arg
ENST00000700203.1:n.1429T>G
ENST00000380152.8:c.9302T>G MANE Select	ENSP00000369497.3:p.Leu3101Arg
ENST00000544455.6:c.9302T>G	ENSP00000439902.1:p.Leu3101Arg
ENST00000614259.2:c.9310T>G	ENSP00000506251.1:n.9310T>G
ENST00000665585.1:c.2180T>G
ENST00000666593.1:c.324T>G	ENSP00000499256.1:n.324T>G
ENST00000680887.1:c.9302T>G	ENSP00000505508.1:p.Leu3101Arg
ENST00000380152.7:c.9302T>G	ENSP00000369497.3:p.Leu3101Arg
ENST00000470094.1:c.259T>G
ENST00000544455.5:c.9302T>G	ENSP00000439902.1:p.Leu3101Arg
NM_000059.3:c.9302T>G , LRG_293t1:c.9302T>G	NP_000050.2:p.Leu3101Arg
XM_011535203.1:c.9302T>G	XP_011533505.1:p.Leu3101Arg
XM_011535204.1:c.9206T>G	XP_011533506.1:p.Leu3069Arg
NM_000059.4:c.9302T>G MANE Select	NP_000050.3:p.Leu3101Arg