Canonical Allele Identifier: CA023708

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 52021
• ClinVar RCV Id: RCV000113538 ; RCV001300745 ; RCV003157312
• dbSNP Id: rs80358855
• MyVariant Identifiers: chr13:g.32914652G>C (hg19) ; chr13:g.32340515G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32340515G>C , CM000675.2:g.32340515G>C	GRCh38
NC_000013.10:g.32914652G>C , CM000675.1:g.32914652G>C	GRCh37
NC_000013.9:g.31812652G>C	NCBI36
NG_012772.3:g.30036G>C , LRG_293:g.30036G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.6160G>C	ENSP00000434898.2:p.Ala2054Pro
ENST00000528762.2:c.6160G>C	ENSP00000433168.2:p.Ala2054Pro
ENST00000530893.7:c.5791G>C	ENSP00000499438.2:p.Ala1931Pro
ENST00000665585.2:c.6160G>C	ENSP00000499570.2:p.Ala2054Pro
ENST00000666593.2:c.6160G>C	ENSP00000499256.2:p.Ala2054Pro
ENST00000700202.2:c.6160G>C	ENSP00000514856.2:p.Ala2054Pro
ENST00000380152.8:c.6160G>C MANE Select	ENSP00000369497.3:p.Ala2054Pro
ENST00000544455.6:c.6160G>C	ENSP00000439902.1:p.Ala2054Pro
ENST00000614259.2:c.6160G>C	ENSP00000506251.1:p.Ala2054Pro
ENST00000680887.1:c.6160G>C	ENSP00000505508.1:p.Ala2054Pro
ENST00000380152.7:c.6160G>C	ENSP00000369497.3:p.Ala2054Pro
ENST00000544455.5:c.6160G>C	ENSP00000439902.1:p.Ala2054Pro
ENST00000614259.1:n.6160G>C
NM_000059.3:c.6160G>C , LRG_293t1:c.6160G>C	NP_000050.2:p.Ala2054Pro
XM_011535203.1:c.6160G>C	XP_011533505.1:p.Ala2054Pro
XM_011535204.1:c.6160G>C	XP_011533506.1:p.Ala2054Pro
XM_011535205.1:c.6160G>C	XP_011533507.1:p.Ala2054Pro
NM_000059.4:c.6160G>C MANE Select	NP_000050.3:p.Ala2054Pro