Canonical Allele Identifier: CA387756184

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 3075859
• ClinVar RCV Id: RCV004018177
• dbSNP Id: rs2137619671
• MyVariant Identifiers: chr13:g.32953532C>T (hg19) ; chr13:g.32379395C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32379395C>T , CM000675.2:g.32379395C>T	GRCh38
NC_000013.10:g.32953532C>T , CM000675.1:g.32953532C>T	GRCh37
NC_000013.9:g.31851532C>T	NCBI36
NG_012772.3:g.68916C>T , LRG_293:g.68916C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8833C>T	ENSP00000434898.2:p.Gln2945Ter
ENST00000528762.2:c.*200C>T	ENSP00000433168.2:n.*200C>T
ENST00000530893.7:c.8464C>T	ENSP00000499438.2:p.Gln2822Ter
ENST00000665585.2:c.*395C>T	ENSP00000499570.2:n.*395C>T
ENST00000666593.2:c.8833C>T	ENSP00000499256.2:p.Gln2945Ter
ENST00000700202.2:c.8833C>T	ENSP00000514856.2:p.Gln2945Ter
ENST00000700202.1:c.1300C>T	ENSP00000514856.1:p.Gln434Ter
ENST00000700203.1:n.960C>T
ENST00000380152.8:c.8833C>T MANE Select	ENSP00000369497.3:p.Gln2945Ter
ENST00000544455.6:c.8833C>T	ENSP00000439902.1:p.Gln2945Ter
ENST00000614259.2:c.8841C>T	ENSP00000506251.1:n.8841C>T
ENST00000665585.1:c.1711C>T
ENST00000680887.1:c.8833C>T	ENSP00000505508.1:p.Gln2945Ter
ENST00000380152.7:c.8833C>T	ENSP00000369497.3:p.Gln2945Ter
ENST00000528762.1:c.395C>T	ENSP00000433168.1:n.395C>T
ENST00000544455.5:c.8833C>T	ENSP00000439902.1:p.Gln2945Ter
NM_000059.3:c.8833C>T , LRG_293t1:c.8833C>T	NP_000050.2:p.Gln2945Ter
XM_011535203.1:c.8833C>T	XP_011533505.1:p.Gln2945Ter
XM_011535204.1:c.8737C>T	XP_011533506.1:p.Gln2913Ter
XM_011535205.1:c.8755-355C>T	XP_011533507.1:n.8755-355C>T
NM_000059.4:c.8833C>T MANE Select	NP_000050.3:p.Gln2945Ter