Canonical Allele Identifier: CA16606828

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 387896
• ClinVar RCV Id: RCV000419809 ; RCV003644982
• dbSNP Id: rs1057522934
• MyVariant Identifiers: chr13:g.32954141T>C (hg19) ; chr13:g.32380004T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32380004T>C , CM000675.2:g.32380004T>C	GRCh38
NC_000013.10:g.32954141T>C , CM000675.1:g.32954141T>C	GRCh37
NC_000013.9:g.31852141T>C	NCBI36
NG_012772.3:g.69525T>C , LRG_293:g.69525T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.9118-3T>C	ENSP00000434898.2:n.9118-3T>C
ENST00000528762.2:c.*485-3T>C	ENSP00000433168.2:n.*485-3T>C
ENST00000530893.7:c.8749-3T>C	ENSP00000499438.2:n.8749-3T>C
ENST00000665585.2:c.*680-3T>C	ENSP00000499570.2:n.*680-3T>C
ENST00000666593.2:c.9118-3T>C	ENSP00000499256.2:n.9118-3T>C
ENST00000700202.2:c.9067-3T>C	ENSP00000514856.2:n.9067-3T>C
ENST00000700202.1:c.1534-3T>C	ENSP00000514856.1:n.1534-3T>C
ENST00000700203.1:n.1245-3T>C
ENST00000380152.8:c.9118-3T>C MANE Select	ENSP00000369497.3:n.9118-3T>C
ENST00000544455.6:c.9118-3T>C	ENSP00000439902.1:n.9118-3T>C
ENST00000614259.2:c.9126-3T>C	ENSP00000506251.1:n.9126-3T>C
ENST00000665585.1:c.1996-3T>C
ENST00000680887.1:c.9118-3T>C	ENSP00000505508.1:n.9118-3T>C
ENST00000380152.7:c.9118-3T>C	ENSP00000369497.3:n.9118-3T>C
ENST00000470094.1:c.75-3T>C
ENST00000544455.5:c.9118-3T>C	ENSP00000439902.1:n.9118-3T>C
NM_000059.3:c.9118-3T>C , LRG_293t1:c.9118-3T>C	NP_000050.2:n.9118-3T>C
XM_011535203.1:c.9118-3T>C	XP_011533505.1:n.9118-3T>C
XM_011535204.1:c.9022-3T>C	XP_011533506.1:n.9022-3T>C
NM_000059.4:c.9118-3T>C MANE Select	NP_000050.3:n.9118-3T>C