Canonical Allele Identifier: CA483270995

Gene: BRCA2

Linked Data

• MyVariant Identifiers: chr13:g.32968851A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32394714A>C , CM000675.2:g.32394714A>C	GRCh38
NC_000013.10:g.32968851A>C , CM000675.1:g.32968851A>C	GRCh37
NC_000013.9:g.31866851A>C	NCBI36
NG_012772.3:g.84235A>C , LRG_293:g.84235A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.9282A>C	ENSP00000434898.2:p.Ser3094=
ENST00000528762.2:c.*649A>C	ENSP00000433168.2:n.*649A>C
ENST00000530893.7:c.8913A>C	ENSP00000499438.2:p.Ser2971=
ENST00000665585.2:c.*844A>C	ENSP00000499570.2:n.*844A>C
ENST00000666593.2:c.*127A>C	ENSP00000499256.2:n.*127A>C
ENST00000700202.2:c.9231A>C	ENSP00000514856.2:p.Ser3077=
ENST00000700202.1:c.1698A>C	ENSP00000514856.1:p.Ser566=
ENST00000700203.1:n.1409A>C
ENST00000380152.8:c.9282A>C MANE Select	ENSP00000369497.3:p.Ser3094=
ENST00000544455.6:c.9282A>C	ENSP00000439902.1:p.Ser3094=
ENST00000614259.2:c.9290A>C	ENSP00000506251.1:n.9290A>C
ENST00000665585.1:c.2160A>C
ENST00000666593.1:c.304A>C	ENSP00000499256.1:n.304A>C
ENST00000680887.1:c.9282A>C	ENSP00000505508.1:p.Ser3094=
ENST00000380152.7:c.9282A>C	ENSP00000369497.3:p.Ser3094=
ENST00000470094.1:c.239A>C
ENST00000544455.5:c.9282A>C	ENSP00000439902.1:p.Ser3094=
NM_000059.3:c.9282A>C , LRG_293t1:c.9282A>C	NP_000050.2:p.Ser3094=
XM_011535203.1:c.9282A>C	XP_011533505.1:p.Ser3094=
XM_011535204.1:c.9186A>C	XP_011533506.1:p.Ser3062=
NM_000059.4:c.9282A>C MANE Select	NP_000050.3:p.Ser3094=