Canonical Allele Identifier: CA2082784249
Gene: BRCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32319282C= , CM000675.2:g.32319282C= GRCh38
NC_000013.10:g.32893419C= , CM000675.1:g.32893419C= GRCh37
NC_000013.9:g.31791419C= NCBI36
NG_012772.3:g.8803C= , LRG_293:g.8803C=
NG_017006.2:g.1082G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000470094.2:c.273C= ENSP00000434898.2:p.Tyr91=
ENST00000528762.2:c.273C= ENSP00000433168.2:p.Tyr91=
ENST00000530893.7:c.-97C= ENSP00000499438.2:n.-97C=
ENST00000665585.2:c.273C= ENSP00000499570.2:p.Tyr91=
ENST00000666593.2:c.273C= ENSP00000499256.2:p.Tyr91=
ENST00000700202.2:c.273C= ENSP00000514856.2:p.Tyr91=
ENST00000700200.1:n.191+2755C=
ENST00000700201.1:c.273C= ENSP00000514855.1:p.Tyr91=
ENST00000380152.8:c.273C= MANE Select ENSP00000369497.3:p.Tyr91=
ENST00000544455.6:c.273C= ENSP00000439902.1:p.Tyr91=
ENST00000614259.2:c.273C= ENSP00000506251.1:p.Tyr91=
ENST00000680887.1:c.273C= ENSP00000505508.1:p.Tyr91=
ENST00000380152.7:c.273C= ENSP00000369497.3:p.Tyr91=
ENST00000530893.6:n.471C=
ENST00000544455.5:c.273C= ENSP00000439902.1:p.Tyr91=
ENST00000614259.1:n.273C=
NM_000059.3:c.273C= , LRG_293t1:c.273C= NP_000050.2:p.Tyr91=
XM_011535203.1:c.273C= XP_011533505.1:p.Tyr91=
XM_011535204.1:c.273C= XP_011533506.1:p.Tyr91=
XM_011535205.1:c.273C= XP_011533507.1:p.Tyr91=
NM_000059.4:c.273C= MANE Select NP_000050.3:p.Tyr91=