Canonical Allele Identifier: CA387752887

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 482978
• ClinVar RCV Id: RCV000562393 ; RCV001369600
• dbSNP Id: rs1555287785
• MyVariant Identifiers: chr13:g.32945205C>T (hg19) ; chr13:g.32371068C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32371068C>T , CM000675.2:g.32371068C>T	GRCh38
NC_000013.10:g.32945205C>T , CM000675.1:g.32945205C>T	GRCh37
NC_000013.9:g.31843205C>T	NCBI36
NG_012772.3:g.60589C>T , LRG_293:g.60589C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8600C>T	ENSP00000434898.2:p.Thr2867Ile
ENST00000528762.2:c.8600C>T	ENSP00000433168.2:p.Thr2867Ile
ENST00000530893.7:c.8231C>T	ENSP00000499438.2:p.Thr2744Ile
ENST00000665585.2:c.8600C>T	ENSP00000499570.2:p.Thr2867Ile
ENST00000666593.2:c.8600C>T	ENSP00000499256.2:p.Thr2867Ile
ENST00000700202.2:c.8600C>T	ENSP00000514856.2:p.Thr2867Ile
ENST00000700202.1:c.1067C>T	ENSP00000514856.1:p.Thr356Ile
ENST00000380152.8:c.8600C>T MANE Select	ENSP00000369497.3:p.Thr2867Ile
ENST00000544455.6:c.8600C>T	ENSP00000439902.1:p.Thr2867Ile
ENST00000614259.2:c.8608C>T	ENSP00000506251.1:n.8608C>T
ENST00000665585.1:c.1165C>T
ENST00000680887.1:c.8600C>T	ENSP00000505508.1:p.Thr2867Ile
ENST00000380152.7:c.8600C>T	ENSP00000369497.3:p.Thr2867Ile
ENST00000528762.1:c.98C>T	ENSP00000433168.1:p.Thr33Ile
ENST00000544455.5:c.8600C>T	ENSP00000439902.1:p.Thr2867Ile
NM_000059.3:c.8600C>T , LRG_293t1:c.8600C>T	NP_000050.2:p.Thr2867Ile
XM_011535203.1:c.8600C>T	XP_011533505.1:p.Thr2867Ile
XM_011535204.1:c.8504C>T	XP_011533506.1:p.Thr2835Ile
XM_011535205.1:c.8600C>T	XP_011533507.1:p.Thr2867Ile
NM_000059.4:c.8600C>T MANE Select	NP_000050.3:p.Thr2867Ile