Canonical Allele Identifier: CA16619758
Gene: BRCA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418086
ClinVar RCV Id: RCV000486734 RCV000661536
dbSNP Id: rs1064793067
MyVariant Identifiers: chr13:g.32929155_32929159del (hg19) chr13:g.32355018_32355022del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32355018_32355022del , CM000675.2:g.32355018_32355022del GRCh38
NC_000013.10:g.32929155_32929159del , CM000675.1:g.32929155_32929159del GRCh37
NC_000013.9:g.31827155_31827159del NCBI36
NG_012772.3:g.44539_44543del , LRG_293:g.44539_44543del

Transcript Alleles

HGVS Amino-acid change
ENST00000470094.2:c.7165_7169del ENSP00000434898.2:p.Arg2389Ter
ENST00000528762.2:c.7165_7169del ENSP00000433168.2:p.Arg2389Ter
ENST00000530893.7:c.6796_6800del ENSP00000499438.2:p.Arg2266Ter
ENST00000665585.2:c.7165_7169del ENSP00000499570.2:p.Arg2389Ter
ENST00000666593.2:c.7165_7169del ENSP00000499256.2:p.Arg2389Ter
ENST00000700202.2:c.7165_7169del ENSP00000514856.2:p.Arg2389Ter
ENST00000380152.8:c.7165_7169del MANE Select ENSP00000369497.3:p.Arg2389Ter
ENST00000544455.6:c.7165_7169del ENSP00000439902.1:p.Arg2389Ter
ENST00000614259.2:c.7165_7169del ENSP00000506251.1:p.Arg2389Ter
ENST00000680887.1:c.7165_7169del ENSP00000505508.1:p.Arg2389Ter
ENST00000380152.7:c.7165_7169del ENSP00000369497.3:p.Arg2389Ter
ENST00000544455.5:c.7165_7169del ENSP00000439902.1:p.Arg2389Ter
ENST00000614259.1:n.7165_7169del
NM_000059.3:c.7165_7169del , LRG_293t1:c.7165_7169del NP_000050.2:p.Arg2389Ter
XM_011535203.1:c.7165_7169del XP_011533505.1:p.Arg2389Ter
XM_011535204.1:c.7069_7073del XP_011533506.1:p.Arg2357Ter
XM_011535205.1:c.7165_7169del XP_011533507.1:p.Arg2389Ter
NM_000059.4:c.7165_7169del MANE Select NP_000050.3:p.Arg2389Ter
Search 100 bp 5'
Search 100 bp 3'