Canonical Allele Identifier: CA2695199243

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 2680248
• ClinVar RCV Id: RCV003474420

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32315555T>C , CM000675.2:g.32315555T>C	GRCh38
NC_000013.10:g.32889692T>C , CM000675.1:g.32889692T>C	GRCh37
NC_000013.9:g.31787692T>C	NCBI36
NG_012772.3:g.5076T>C , LRG_293:g.5076T>C
NG_017006.1:g.1400A>G
NG_017006.2:g.4809A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.-152T>C	ENSP00000434898.2:n.-152T>C
ENST00000528762.2:c.-152T>C	ENSP00000433168.2:n.-152T>C
ENST00000530893.7:c.-517T>C	ENSP00000499438.2:n.-517T>C
ENST00000665585.2:c.-152T>C	ENSP00000499570.2:n.-152T>C
ENST00000666593.2:c.-152T>C	ENSP00000499256.2:n.-152T>C
ENST00000700202.2:c.-152T>C	ENSP00000514856.2:n.-152T>C
ENST00000380152.8:c.-152T>C MANE Select	ENSP00000369497.3:n.-152T>C
ENST00000544455.6:c.-40+410T>C	ENSP00000439902.1:n.-40+410T>C
ENST00000380152.7:c.-152T>C	ENSP00000369497.3:n.-152T>C
ENST00000530893.6:n.51T>C
ENST00000544455.5:c.-152T>C	ENSP00000439902.1:n.-152T>C
NM_000059.3:c.-152T>C , LRG_293t1:c.-152T>C	NP_000050.2:n.-152T>C
XM_011535203.1:c.-40+410T>C	XP_011533505.1:n.-40+410T>C
XM_011535204.1:c.-152T>C	XP_011533506.1:n.-152T>C
XM_011535205.1:c.-152T>C	XP_011533507.1:n.-152T>C
NM_000059.4:c.-152T>C MANE Select	NP_000050.3:n.-152T>C