Canonical Allele Identifier: CA025605
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 52566
dbSNP Id: rs397507981

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32370434G>A , CM000675.2:g.32370434G>A GRCh38
NC_000013.10:g.32944571G>A , CM000675.1:g.32944571G>A GRCh37
NC_000013.9:g.31842571G>A NCBI36
NG_012772.3:g.59955G>A , LRG_293:g.59955G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8364G>A ENSP00000434898.2:p.Trp2788Ter
ENST00000528762.2:c.8364G>A ENSP00000433168.2:p.Trp2788Ter
ENST00000530893.7:c.7995G>A ENSP00000499438.2:p.Trp2665Ter
ENST00000665585.2:c.8364G>A ENSP00000499570.2:p.Trp2788Ter
ENST00000666593.2:c.8364G>A ENSP00000499256.2:p.Trp2788Ter
ENST00000700202.2:c.8364G>A ENSP00000514856.2:p.Trp2788Ter
ENST00000700202.1:c.831G>A ENSP00000514856.1:p.Trp277Ter
ENST00000380152.8:c.8364G>A MANE Select ENSP00000369497.3:p.Trp2788Ter
ENST00000544455.6:c.8364G>A ENSP00000439902.1:p.Trp2788Ter
ENST00000614259.2:c.8372G>A ENSP00000506251.1:n.8372G>A
ENST00000665585.1:c.929G>A
ENST00000680887.1:c.8364G>A ENSP00000505508.1:p.Trp2788Ter
ENST00000380152.7:c.8364G>A ENSP00000369497.3:p.Trp2788Ter
ENST00000544455.5:c.8364G>A ENSP00000439902.1:p.Trp2788Ter
NM_000059.3:c.8364G>A , LRG_293t1:c.8364G>A NP_000050.2:p.Trp2788Ter
XM_011535203.1:c.8364G>A XP_011533505.1:p.Trp2788Ter
XM_011535204.1:c.8268G>A XP_011533506.1:p.Trp2756Ter
XM_011535205.1:c.8364G>A XP_011533507.1:p.Trp2788Ter
NM_000059.4:c.8364G>A MANE Select NP_000050.3:p.Trp2788Ter