Canonical Allele Identifier: CA483261012

Gene: BRCA2

Linked Data

• dbSNP Id: rs80359799
• gnomAD v2: 13-32936801-A-C
• gnomAD v3: 13-32362664-A-C
• gnomAD v4: 13-32362664-A-C
• MyVariant Identifiers: chr13:g.32936801A>C (hg19) ; chr13:g.32362664A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32362664A>C , CM000675.2:g.32362664A>C	GRCh38
NC_000013.10:g.32936801A>C , CM000675.1:g.32936801A>C	GRCh37
NC_000013.9:g.31834801A>C	NCBI36
NG_012772.3:g.52185A>C , LRG_293:g.52185A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7947A>C	ENSP00000434898.2:p.Pro2649=
ENST00000528762.2:c.7947A>C	ENSP00000433168.2:p.Pro2649=
ENST00000530893.7:c.7578A>C	ENSP00000499438.2:p.Pro2526=
ENST00000665585.2:c.7947A>C	ENSP00000499570.2:p.Pro2649=
ENST00000666593.2:c.7947A>C	ENSP00000499256.2:p.Pro2649=
ENST00000700202.2:c.7947A>C	ENSP00000514856.2:p.Pro2649=
ENST00000700202.1:c.414A>C	ENSP00000514856.1:p.Pro138=
ENST00000380152.8:c.7947A>C MANE Select	ENSP00000369497.3:p.Pro2649=
ENST00000544455.6:c.7947A>C	ENSP00000439902.1:p.Pro2649=
ENST00000614259.2:c.7955A>C	ENSP00000506251.1:n.7955A>C
ENST00000665585.1:c.512A>C
ENST00000680887.1:c.7947A>C	ENSP00000505508.1:p.Pro2649=
ENST00000380152.7:c.7947A>C	ENSP00000369497.3:p.Pro2649=
ENST00000544455.5:c.7947A>C	ENSP00000439902.1:p.Pro2649=
NM_000059.3:c.7947A>C , LRG_293t1:c.7947A>C	NP_000050.2:p.Pro2649=
XM_011535203.1:c.7947A>C	XP_011533505.1:p.Pro2649=
XM_011535204.1:c.7851A>C	XP_011533506.1:p.Pro2617=
XM_011535205.1:c.7947A>C	XP_011533507.1:p.Pro2649=
NM_000059.4:c.7947A>C MANE Select	NP_000050.3:p.Pro2649=