Canonical Allele Identifier: CA483261200

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 822373
• ClinVar RCV Id: RCV001017680
• dbSNP Id: rs1593930274
• MyVariant Identifiers: chr13:g.32944601T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32370464T>G , CM000675.2:g.32370464T>G	GRCh38
NC_000013.10:g.32944601T>G , CM000675.1:g.32944601T>G	GRCh37
NC_000013.9:g.31842601T>G	NCBI36
NG_012772.3:g.59985T>G , LRG_293:g.59985T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8394T>G	ENSP00000434898.2:p.Pro2798=
ENST00000528762.2:c.8394T>G	ENSP00000433168.2:p.Pro2798=
ENST00000530893.7:c.8025T>G	ENSP00000499438.2:p.Pro2675=
ENST00000665585.2:c.8394T>G	ENSP00000499570.2:p.Pro2798=
ENST00000666593.2:c.8394T>G	ENSP00000499256.2:p.Pro2798=
ENST00000700202.2:c.8394T>G	ENSP00000514856.2:p.Pro2798=
ENST00000700202.1:c.861T>G	ENSP00000514856.1:p.Pro287=
ENST00000380152.8:c.8394T>G MANE Select	ENSP00000369497.3:p.Pro2798=
ENST00000544455.6:c.8394T>G	ENSP00000439902.1:p.Pro2798=
ENST00000614259.2:c.8402T>G	ENSP00000506251.1:n.8402T>G
ENST00000665585.1:c.959T>G
ENST00000680887.1:c.8394T>G	ENSP00000505508.1:p.Pro2798=
ENST00000380152.7:c.8394T>G	ENSP00000369497.3:p.Pro2798=
ENST00000544455.5:c.8394T>G	ENSP00000439902.1:p.Pro2798=
NM_000059.3:c.8394T>G , LRG_293t1:c.8394T>G	NP_000050.2:p.Pro2798=
XM_011535203.1:c.8394T>G	XP_011533505.1:p.Pro2798=
XM_011535204.1:c.8298T>G	XP_011533506.1:p.Pro2766=
XM_011535205.1:c.8394T>G	XP_011533507.1:p.Pro2798=
NM_000059.4:c.8394T>G MANE Select	NP_000050.3:p.Pro2798=