Canonical Allele Identifier: CA483439694
Gene: BRCA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.32953636A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32379499A>G , CM000675.2:g.32379499A>G GRCh38
NC_000013.10:g.32953636A>G , CM000675.1:g.32953636A>G GRCh37
NC_000013.9:g.31851636A>G NCBI36
NG_012772.3:g.69020A>G , LRG_293:g.69020A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.8937A>G ENSP00000434898.2:p.Lys2979=
ENST00000528762.2:c.*304A>G ENSP00000433168.2:n.*304A>G
ENST00000530893.7:c.8568A>G ENSP00000499438.2:p.Lys2856=
ENST00000665585.2:c.*499A>G ENSP00000499570.2:n.*499A>G
ENST00000666593.2:c.8937A>G ENSP00000499256.2:p.Lys2979=
ENST00000700202.2:c.8937A>G ENSP00000514856.2:p.Lys2979=
ENST00000700202.1:c.1404A>G ENSP00000514856.1:p.Lys468=
ENST00000700203.1:n.1064A>G
ENST00000380152.8:c.8937A>G MANE Select ENSP00000369497.3:p.Lys2979=
ENST00000544455.6:c.8937A>G ENSP00000439902.1:p.Lys2979=
ENST00000614259.2:c.8945A>G ENSP00000506251.1:n.8945A>G
ENST00000665585.1:c.1815A>G
ENST00000680887.1:c.8937A>G ENSP00000505508.1:p.Lys2979=
ENST00000380152.7:c.8937A>G ENSP00000369497.3:p.Lys2979=
ENST00000544455.5:c.8937A>G ENSP00000439902.1:p.Lys2979=
NM_000059.3:c.8937A>G , LRG_293t1:c.8937A>G NP_000050.2:p.Lys2979=
XM_011535203.1:c.8937A>G XP_011533505.1:p.Lys2979=
XM_011535204.1:c.8841A>G XP_011533506.1:p.Lys2947=
XM_011535205.1:c.8755-251A>G XP_011533507.1:n.8755-251A>G
NM_000059.4:c.8937A>G MANE Select NP_000050.3:p.Lys2979=