Canonical Allele Identifier: CA387746983

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 482993
• ClinVar RCV Id: RCV000575468 ; RCV000818024 ; RCV001171394 ; RCV003459345
• dbSNP Id: rs1555286821
• gnomAD v4: 13-32362537-C-T
• MyVariant Identifiers: chr13:g.32936674C>T (hg19) ; chr13:g.32362537C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362537C>T , CM000675.2:g.32362537C>T	GRCh38
NC_000013.10:g.32936674C>T , CM000675.1:g.32936674C>T	GRCh37
NC_000013.9:g.31834674C>T	NCBI36
NG_012772.3:g.52058C>T , LRG_293:g.52058C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.7820C>T	ENSP00000434898.2:p.Thr2607Ile
ENST00000528762.2:c.7820C>T	ENSP00000433168.2:p.Thr2607Ile
ENST00000530893.7:c.7451C>T	ENSP00000499438.2:p.Thr2484Ile
ENST00000665585.2:c.7820C>T	ENSP00000499570.2:p.Thr2607Ile
ENST00000666593.2:c.7820C>T	ENSP00000499256.2:p.Thr2607Ile
ENST00000700202.2:c.7820C>T	ENSP00000514856.2:p.Thr2607Ile
ENST00000700202.1:c.287C>T	ENSP00000514856.1:p.Thr96Ile
ENST00000380152.8:c.7820C>T MANE Select	ENSP00000369497.3:p.Thr2607Ile
ENST00000544455.6:c.7820C>T	ENSP00000439902.1:p.Thr2607Ile
ENST00000614259.2:c.7828C>T	ENSP00000506251.1:p.Leu2610Phe
ENST00000665585.1:c.385C>T
ENST00000680887.1:c.7820C>T	ENSP00000505508.1:p.Thr2607Ile
ENST00000380152.7:c.7820C>T	ENSP00000369497.3:p.Thr2607Ile
ENST00000544455.5:c.7820C>T	ENSP00000439902.1:p.Thr2607Ile
ENST00000614259.1:n.7828C>T
NM_000059.3:c.7820C>T , LRG_293t1:c.7820C>T	NP_000050.2:p.Thr2607Ile
XM_011535203.1:c.7820C>T	XP_011533505.1:p.Thr2607Ile
XM_011535204.1:c.7724C>T	XP_011533506.1:p.Thr2575Ile
XM_011535205.1:c.7820C>T	XP_011533507.1:p.Thr2607Ile
NM_000059.4:c.7820C>T MANE Select	NP_000050.3:p.Thr2607Ile