Canonical Allele Identifier: CA483440160

Gene: BRCA2

Linked Data

• MyVariant Identifiers: chr13:g.32972664A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398527A>C , CM000675.2:g.32398527A>C	GRCh38
NC_000013.10:g.32972664A>C , CM000675.1:g.32972664A>C	GRCh37
NC_000013.9:g.31870664A>C	NCBI36
NG_012772.3:g.88048A>C , LRG_293:g.88048A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*537A>C	ENSP00000434898.2:n.*537A>C
ENST00000528762.2:c.*1381A>C	ENSP00000433168.2:n.*1381A>C
ENST00000530893.7:c.9645A>C	ENSP00000499438.2:p.Ser3215=
ENST00000665585.2:c.*1576A>C	ENSP00000499570.2:n.*1576A>C
ENST00000700202.2:c.9963A>C	ENSP00000514856.2:p.Ser3321=
ENST00000700202.1:c.2430A>C	ENSP00000514856.1:p.Ser810=
ENST00000700203.1:n.2141A>C
ENST00000380152.8:c.10014A>C MANE Select	ENSP00000369497.3:p.Ser3338=
ENST00000544455.6:c.10014A>C	ENSP00000439902.1:p.Ser3338=
ENST00000614259.2:c.10022A>C	ENSP00000506251.1:n.10022A>C
ENST00000680887.1:c.10014A>C	ENSP00000505508.1:p.Ser3338=
ENST00000380152.7:c.10014A>C	ENSP00000369497.3:p.Ser3338=
ENST00000544455.5:c.10014A>C	ENSP00000439902.1:p.Ser3338=
NM_000059.3:c.10014A>C , LRG_293t1:c.10014A>C	NP_000050.2:p.Ser3338=
XM_011535203.1:c.10014A>C	XP_011533505.1:p.Ser3338=
XM_011535204.1:c.9918A>C	XP_011533506.1:p.Ser3306=
NM_000059.4:c.10014A>C MANE Select	NP_000050.3:p.Ser3338=