Canonical Allele Identifier: CA336954

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 215601
• ClinVar RCV Id: RCV000197063 ; RCV000494866 ; RCV000568726
• dbSNP Id: rs863224303
• gnomAD v2: 13-32893368-G-C
• gnomAD v3: 13-32319231-G-C
• gnomAD v4: 13-32319231-G-C
• MyVariant Identifiers: chr13:g.32893368G>C (hg19) ; chr13:g.32319231G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32319231G>C , CM000675.2:g.32319231G>C	GRCh38
NC_000013.10:g.32893368G>C , CM000675.1:g.32893368G>C	GRCh37
NC_000013.9:g.31791368G>C	NCBI36
NG_012772.3:g.8752G>C , LRG_293:g.8752G>C
NG_017006.2:g.1133C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.222G>C	ENSP00000434898.2:p.Leu74=
ENST00000528762.2:c.222G>C	ENSP00000433168.2:p.Leu74=
ENST00000530893.7:c.-148G>C	ENSP00000499438.2:n.-148G>C
ENST00000665585.2:c.222G>C	ENSP00000499570.2:p.Leu74=
ENST00000666593.2:c.222G>C	ENSP00000499256.2:p.Leu74=
ENST00000700202.2:c.222G>C	ENSP00000514856.2:p.Leu74=
ENST00000700200.1:n.191+2704G>C
ENST00000700201.1:c.222G>C	ENSP00000514855.1:p.Leu74=
ENST00000380152.8:c.222G>C MANE Select	ENSP00000369497.3:p.Leu74=
ENST00000544455.6:c.222G>C	ENSP00000439902.1:p.Leu74=
ENST00000614259.2:c.222G>C	ENSP00000506251.1:p.Leu74=
ENST00000680887.1:c.222G>C	ENSP00000505508.1:p.Leu74=
ENST00000380152.7:c.222G>C	ENSP00000369497.3:p.Leu74=
ENST00000530893.6:n.420G>C
ENST00000544455.5:c.222G>C	ENSP00000439902.1:p.Leu74=
ENST00000614259.1:n.222G>C
NM_000059.3:c.222G>C , LRG_293t1:c.222G>C	NP_000050.2:p.Leu74=
XM_011535203.1:c.222G>C	XP_011533505.1:p.Leu74=
XM_011535204.1:c.222G>C	XP_011533506.1:p.Leu74=
XM_011535205.1:c.222G>C	XP_011533507.1:p.Leu74=
NM_000059.4:c.222G>C MANE Select	NP_000050.3:p.Leu74=