Canonical Allele Identifier: CA387754048

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 1037114
• ClinVar RCV Id: RCV001340219 ; RCV002412065
• dbSNP Id: rs1566215668
• gnomAD v3: 13-32319086-C-G
• gnomAD v4: 13-32319086-C-G
• MyVariant Identifiers: chr13:g.32893223C>G (hg19) ; chr13:g.32319086C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32319086C>G , CM000675.2:g.32319086C>G	GRCh38
NC_000013.10:g.32893223C>G , CM000675.1:g.32893223C>G	GRCh37
NC_000013.9:g.31791223C>G	NCBI36
NG_012772.3:g.8607C>G , LRG_293:g.8607C>G
NG_017006.2:g.1278G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.77C>G	ENSP00000434898.2:p.Pro26Arg
ENST00000528762.2:c.77C>G	ENSP00000433168.2:p.Pro26Arg
ENST00000530893.7:c.-293C>G	ENSP00000499438.2:n.-293C>G
ENST00000665585.2:c.77C>G	ENSP00000499570.2:p.Pro26Arg
ENST00000666593.2:c.77C>G	ENSP00000499256.2:p.Pro26Arg
ENST00000700202.2:c.77C>G	ENSP00000514856.2:p.Pro26Arg
ENST00000700200.1:n.191+2559C>G
ENST00000700201.1:c.77C>G	ENSP00000514855.1:p.Pro26Arg
ENST00000380152.8:c.77C>G MANE Select	ENSP00000369497.3:p.Pro26Arg
ENST00000544455.6:c.77C>G	ENSP00000439902.1:p.Pro26Arg
ENST00000614259.2:c.77C>G	ENSP00000506251.1:p.Pro26Arg
ENST00000680887.1:c.77C>G	ENSP00000505508.1:p.Pro26Arg
ENST00000380152.7:c.77C>G	ENSP00000369497.3:p.Pro26Arg
ENST00000530893.6:n.275C>G
ENST00000544455.5:c.77C>G	ENSP00000439902.1:p.Pro26Arg
ENST00000614259.1:n.77C>G
NM_000059.3:c.77C>G , LRG_293t1:c.77C>G	NP_000050.2:p.Pro26Arg
XM_011535203.1:c.77C>G	XP_011533505.1:p.Pro26Arg
XM_011535204.1:c.77C>G	XP_011533506.1:p.Pro26Arg
XM_011535205.1:c.77C>G	XP_011533507.1:p.Pro26Arg
NM_000059.4:c.77C>G MANE Select	NP_000050.3:p.Pro26Arg