Canonical Allele Identifier: CA483439453
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1757330
ClinVar RCV Id: RCV002367476
dbSNP Id: rs730881593
MyVariant Identifiers: chr13:g.32929127A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32354990A>T , CM000675.2:g.32354990A>T GRCh38
NC_000013.10:g.32929127A>T , CM000675.1:g.32929127A>T GRCh37
NC_000013.9:g.31827127A>T NCBI36
NG_012772.3:g.44511A>T , LRG_293:g.44511A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.7137A>T ENSP00000434898.2:p.Gly2379=
ENST00000528762.2:c.7137A>T ENSP00000433168.2:p.Gly2379=
ENST00000530893.7:c.6768A>T ENSP00000499438.2:p.Gly2256=
ENST00000665585.2:c.7137A>T ENSP00000499570.2:p.Gly2379=
ENST00000666593.2:c.7137A>T ENSP00000499256.2:p.Gly2379=
ENST00000700202.2:c.7137A>T ENSP00000514856.2:p.Gly2379=
ENST00000380152.8:c.7137A>T MANE Select ENSP00000369497.3:p.Gly2379=
ENST00000544455.6:c.7137A>T ENSP00000439902.1:p.Gly2379=
ENST00000614259.2:c.7137A>T ENSP00000506251.1:p.Gly2379=
ENST00000680887.1:c.7137A>T ENSP00000505508.1:p.Gly2379=
ENST00000380152.7:c.7137A>T ENSP00000369497.3:p.Gly2379=
ENST00000544455.5:c.7137A>T ENSP00000439902.1:p.Gly2379=
ENST00000614259.1:n.7137A>T
NM_000059.3:c.7137A>T , LRG_293t1:c.7137A>T NP_000050.2:p.Gly2379=
XM_011535203.1:c.7137A>T XP_011533505.1:p.Gly2379=
XM_011535204.1:c.7041A>T XP_011533506.1:p.Gly2347=
XM_011535205.1:c.7137A>T XP_011533507.1:p.Gly2379=
NM_000059.4:c.7137A>T MANE Select NP_000050.3:p.Gly2379=