Canonical Allele Identifier: CA387743792
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2451545
ClinVar RCV Id: RCV003187241
dbSNP Id: rs2137563167

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32356564A>T , CM000675.2:g.32356564A>T GRCh38
NC_000013.10:g.32930701A>T , CM000675.1:g.32930701A>T GRCh37
NC_000013.9:g.31828701A>T NCBI36
NG_012772.3:g.46085A>T , LRG_293:g.46085A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.7572A>T ENSP00000434898.2:p.Lys2524Asn
ENST00000528762.2:c.7572A>T ENSP00000433168.2:p.Lys2524Asn
ENST00000530893.7:c.7203A>T ENSP00000499438.2:p.Lys2401Asn
ENST00000665585.2:c.7572A>T ENSP00000499570.2:p.Lys2524Asn
ENST00000666593.2:c.7572A>T ENSP00000499256.2:p.Lys2524Asn
ENST00000700202.2:c.7572A>T ENSP00000514856.2:p.Lys2524Asn
ENST00000700202.1:c.39A>T ENSP00000514856.1:p.Lys13Asn
ENST00000380152.8:c.7572A>T MANE Select ENSP00000369497.3:p.Lys2524Asn
ENST00000544455.6:c.7572A>T ENSP00000439902.1:p.Lys2524Asn
ENST00000614259.2:c.7572A>T ENSP00000506251.1:p.Lys2524Asn
ENST00000665585.1:c.137A>T
ENST00000680887.1:c.7572A>T ENSP00000505508.1:p.Lys2524Asn
ENST00000380152.7:c.7572A>T ENSP00000369497.3:p.Lys2524Asn
ENST00000544455.5:c.7572A>T ENSP00000439902.1:p.Lys2524Asn
ENST00000614259.1:n.7572A>T
NM_000059.3:c.7572A>T , LRG_293t1:c.7572A>T NP_000050.2:p.Lys2524Asn
XM_011535203.1:c.7572A>T XP_011533505.1:p.Lys2524Asn
XM_011535204.1:c.7476A>T XP_011533506.1:p.Lys2492Asn
XM_011535205.1:c.7572A>T XP_011533507.1:p.Lys2524Asn
NM_000059.4:c.7572A>T MANE Select NP_000050.3:p.Lys2524Asn