Canonical Allele Identifier: CA2082775271
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32316425T= , CM000675.2:g.32316425T= GRCh38
NC_000013.10:g.32890562T= , CM000675.1:g.32890562T= GRCh37
NC_000013.9:g.31788562T= NCBI36
NG_012772.3:g.5946T= , LRG_293:g.5946T=
NG_017006.1:g.530A=
NG_017006.2:g.3939A=

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.-36T= ENSP00000434898.2:n.-36T=
ENST00000528762.2:c.-36T= ENSP00000433168.2:n.-36T=
ENST00000530893.7:c.-401T= ENSP00000499438.2:n.-401T=
ENST00000665585.2:c.-36T= ENSP00000499570.2:n.-36T=
ENST00000666593.2:c.-36T= ENSP00000499256.2:n.-36T=
ENST00000700202.2:c.-36T= ENSP00000514856.2:n.-36T=
ENST00000700199.1:n.89T=
ENST00000700200.1:n.89T=
ENST00000700201.1:c.-36T= ENSP00000514855.1:n.-36T=
ENST00000380152.8:c.-36T= MANE Select ENSP00000369497.3:n.-36T=
ENST00000544455.6:c.-36T= ENSP00000439902.1:n.-36T=
ENST00000680887.1:c.-36T= ENSP00000505508.1:n.-36T=
ENST00000380152.7:c.-36T= ENSP00000369497.3:n.-36T=
ENST00000530893.6:n.167T=
ENST00000544455.5:c.-36T= ENSP00000439902.1:n.-36T=
NM_000059.3:c.-36T= , LRG_293t1:c.-36T= NP_000050.2:n.-36T=
XM_011535203.1:c.-36T= XP_011533505.1:n.-36T=
XM_011535204.1:c.-36T= XP_011533506.1:n.-36T=
XM_011535205.1:c.-36T= XP_011533507.1:n.-36T=
NM_000059.4:c.-36T= MANE Select NP_000050.3:n.-36T=