Canonical Allele Identifier: CA10577476

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 234506
• ClinVar RCV Id: RCV000220651 ; RCV000462700 ; RCV000566954 ; RCV000661386
• dbSNP Id: rs876661056
• MyVariant Identifiers: chr13:g.32913626G>T (hg19) ; chr13:g.32339489G>T (hg38)
• PubMed: PMID:20609468

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32339489G>T , CM000675.2:g.32339489G>T	GRCh38
NC_000013.10:g.32913626G>T , CM000675.1:g.32913626G>T	GRCh37
NC_000013.9:g.31811626G>T	NCBI36
NG_012772.3:g.29010G>T , LRG_293:g.29010G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.5134G>T	ENSP00000434898.2:p.Gly1712Ter
ENST00000528762.2:c.5134G>T	ENSP00000433168.2:p.Gly1712Ter
ENST00000530893.7:c.4765G>T	ENSP00000499438.2:p.Gly1589Ter
ENST00000665585.2:c.5134G>T	ENSP00000499570.2:p.Gly1712Ter
ENST00000666593.2:c.5134G>T	ENSP00000499256.2:p.Gly1712Ter
ENST00000700202.2:c.5134G>T	ENSP00000514856.2:p.Gly1712Ter
ENST00000380152.8:c.5134G>T MANE Select	ENSP00000369497.3:p.Gly1712Ter
ENST00000544455.6:c.5134G>T	ENSP00000439902.1:p.Gly1712Ter
ENST00000614259.2:c.5134G>T	ENSP00000506251.1:p.Gly1712Ter
ENST00000680887.1:c.5134G>T	ENSP00000505508.1:p.Gly1712Ter
ENST00000380152.7:c.5134G>T	ENSP00000369497.3:p.Gly1712Ter
ENST00000544455.5:c.5134G>T	ENSP00000439902.1:p.Gly1712Ter
ENST00000614259.1:n.5134G>T
NM_000059.3:c.5134G>T , LRG_293t1:c.5134G>T	NP_000050.2:p.Gly1712Ter
XM_011535203.1:c.5134G>T	XP_011533505.1:p.Gly1712Ter
XM_011535204.1:c.5134G>T	XP_011533506.1:p.Gly1712Ter
XM_011535205.1:c.5134G>T	XP_011533507.1:p.Gly1712Ter
NM_000059.4:c.5134G>T MANE Select	NP_000050.3:p.Gly1712Ter