Canonical Allele Identifier: CA348339

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 220004
• ClinVar RCV Id: RCV000495664 ; RCV000573059 ; RCV000758923 ; RCV001082945
• dbSNP Id: rs768731187
• ExAC: 13:32903581 C / T
• gnomAD v2: 13-32903581-C-T
• gnomAD v3: 13-32329444-C-T
• gnomAD v4: 13-32329444-C-T
• MyVariant Identifiers: chr13:g.32903581C>T (hg19) ; chr13:g.32329444C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32329444C>T , CM000675.2:g.32329444C>T	GRCh38
NC_000013.10:g.32903581C>T , CM000675.1:g.32903581C>T	GRCh37
NC_000013.9:g.31801581C>T	NCBI36
NG_012772.3:g.18965C>T , LRG_293:g.18965C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.633C>T	ENSP00000434898.2:p.Val211=
ENST00000528762.2:c.633C>T	ENSP00000433168.2:p.Val211=
ENST00000530893.7:c.264C>T	ENSP00000499438.2:p.Val88=
ENST00000665585.2:c.633C>T	ENSP00000499570.2:p.Val211=
ENST00000666593.2:c.633C>T	ENSP00000499256.2:p.Val211=
ENST00000700202.2:c.633C>T	ENSP00000514856.2:p.Val211=
ENST00000700201.1:c.*412C>T	ENSP00000514855.1:n.*412C>T
ENST00000380152.8:c.633C>T MANE Select	ENSP00000369497.3:p.Val211=
ENST00000544455.6:c.633C>T	ENSP00000439902.1:p.Val211=
ENST00000614259.2:c.633C>T	ENSP00000506251.1:p.Val211=
ENST00000680887.1:c.633C>T	ENSP00000505508.1:p.Val211=
ENST00000380152.7:c.633C>T	ENSP00000369497.3:p.Val211=
ENST00000530893.6:n.831C>T
ENST00000544455.5:c.633C>T	ENSP00000439902.1:p.Val211=
ENST00000614259.1:n.633C>T
NM_000059.3:c.633C>T , LRG_293t1:c.633C>T	NP_000050.2:p.Val211=
XM_011535203.1:c.633C>T	XP_011533505.1:p.Val211=
XM_011535204.1:c.633C>T	XP_011533506.1:p.Val211=
XM_011535205.1:c.633C>T	XP_011533507.1:p.Val211=
NM_000059.4:c.633C>T MANE Select	NP_000050.3:p.Val211=