Canonical Allele Identifier: CA025748
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 52643
dbSNP Id: rs56268579

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32376644A>G , CM000675.2:g.32376644A>G GRCh38
NC_000013.10:g.32950781A>G , CM000675.1:g.32950781A>G GRCh37
NC_000013.9:g.31848781A>G NCBI36
NG_012772.3:g.66165A>G , LRG_293:g.66165A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.8633-26A>G ENSP00000434898.2:n.8633-26A>G
ENST00000528762.2:c.8697-26A>G ENSP00000433168.2:n.8697-26A>G
ENST00000530893.7:c.8264-26A>G ENSP00000499438.2:n.8264-26A>G
ENST00000665585.2:c.*195-26A>G ENSP00000499570.2:n.*195-26A>G
ENST00000666593.2:c.8633-26A>G ENSP00000499256.2:n.8633-26A>G
ENST00000700202.2:c.8633-26A>G ENSP00000514856.2:n.8633-26A>G
ENST00000700202.1:c.1100-26A>G ENSP00000514856.1:n.1100-26A>G
ENST00000700203.1:n.734A>G
ENST00000380152.8:c.8633-26A>G MANE Select ENSP00000369497.3:n.8633-26A>G
ENST00000544455.6:c.8633-26A>G ENSP00000439902.1:n.8633-26A>G
ENST00000614259.2:c.8641-26A>G ENSP00000506251.1:n.8641-26A>G
ENST00000665585.1:c.1511-26A>G
ENST00000680887.1:c.8633-26A>G ENSP00000505508.1:n.8633-26A>G
ENST00000380152.7:c.8633-26A>G ENSP00000369497.3:n.8633-26A>G
ENST00000528762.1:c.195-26A>G ENSP00000433168.1:n.195-26A>G
ENST00000544455.5:c.8633-26A>G ENSP00000439902.1:n.8633-26A>G
NM_000059.3:c.8633-26A>G , LRG_293t1:c.8633-26A>G NP_000050.2:n.8633-26A>G
XM_011535203.1:c.8633-26A>G XP_011533505.1:n.8633-26A>G
XM_011535204.1:c.8537-26A>G XP_011533506.1:n.8537-26A>G
XM_011535205.1:c.8633-26A>G XP_011533507.1:n.8633-26A>G
NM_000059.4:c.8633-26A>G MANE Select NP_000050.3:n.8633-26A>G