Canonical Allele Identifier: CA387755697

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 1686522
• ClinVar RCV Id: RCV002247035
• dbSNP Id: rs1454684155
• MyVariant Identifiers: chr13:g.32953454G>T (hg19) ; chr13:g.32379317G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379317G>T , CM000675.2:g.32379317G>T	GRCh38
NC_000013.10:g.32953454G>T , CM000675.1:g.32953454G>T	GRCh37
NC_000013.9:g.31851454G>T	NCBI36
NG_012772.3:g.68838G>T , LRG_293:g.68838G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8755G>T	ENSP00000434898.2:p.Gly2919Cys
ENST00000528762.2:c.*122G>T	ENSP00000433168.2:n.*122G>T
ENST00000530893.7:c.8386G>T	ENSP00000499438.2:p.Gly2796Cys
ENST00000665585.2:c.*317G>T	ENSP00000499570.2:n.*317G>T
ENST00000666593.2:c.8755G>T	ENSP00000499256.2:p.Gly2919Cys
ENST00000700202.2:c.8755G>T	ENSP00000514856.2:p.Gly2919Cys
ENST00000700202.1:c.1222G>T	ENSP00000514856.1:p.Gly408Cys
ENST00000700203.1:n.882G>T
ENST00000380152.8:c.8755G>T MANE Select	ENSP00000369497.3:p.Gly2919Cys
ENST00000544455.6:c.8755G>T	ENSP00000439902.1:p.Gly2919Cys
ENST00000614259.2:c.8763G>T	ENSP00000506251.1:n.8763G>T
ENST00000665585.1:c.1633G>T
ENST00000680887.1:c.8755G>T	ENSP00000505508.1:p.Gly2919Cys
ENST00000380152.7:c.8755G>T	ENSP00000369497.3:p.Gly2919Cys
ENST00000528762.1:c.317G>T	ENSP00000433168.1:n.317G>T
ENST00000544455.5:c.8755G>T	ENSP00000439902.1:p.Gly2919Cys
NM_000059.3:c.8755G>T , LRG_293t1:c.8755G>T	NP_000050.2:p.Gly2919Cys
XM_011535203.1:c.8755G>T	XP_011533505.1:p.Gly2919Cys
XM_011535204.1:c.8659G>T	XP_011533506.1:p.Gly2887Cys
XM_011535205.1:c.8755-433G>T	XP_011533507.1:n.8755-433G>T
NM_000059.4:c.8755G>T MANE Select	NP_000050.3:p.Gly2919Cys