Canonical Allele Identifier: CA2727803970

Gene: BRCA2

Linked Data

• dbSNP Id: rs2138695504

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32315621T>G , CM000675.2:g.32315621T>G	GRCh38
NC_000013.10:g.32889758T>G , CM000675.1:g.32889758T>G	GRCh37
NC_000013.9:g.31787758T>G	NCBI36
NG_012772.3:g.5142T>G , LRG_293:g.5142T>G
NG_017006.1:g.1334A>C
NG_017006.2:g.4743A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.-86T>G	ENSP00000434898.2:n.-86T>G
ENST00000528762.2:c.-86T>G	ENSP00000433168.2:n.-86T>G
ENST00000530893.7:c.-451T>G	ENSP00000499438.2:n.-451T>G
ENST00000665585.2:c.-86T>G	ENSP00000499570.2:n.-86T>G
ENST00000666593.2:c.-86T>G	ENSP00000499256.2:n.-86T>G
ENST00000700202.2:c.-86T>G	ENSP00000514856.2:n.-86T>G
ENST00000700199.1:n.39T>G
ENST00000700200.1:n.39T>G
ENST00000700201.1:c.-86T>G	ENSP00000514855.1:n.-86T>G
ENST00000380152.8:c.-86T>G MANE Select	ENSP00000369497.3:n.-86T>G
ENST00000544455.6:c.-40+476T>G	ENSP00000439902.1:n.-40+476T>G
ENST00000380152.7:c.-86T>G	ENSP00000369497.3:n.-86T>G
ENST00000530893.6:n.117T>G
ENST00000544455.5:c.-86T>G	ENSP00000439902.1:n.-86T>G
NM_000059.3:c.-86T>G , LRG_293t1:c.-86T>G	NP_000050.2:n.-86T>G
XM_011535203.1:c.-40+476T>G	XP_011533505.1:n.-40+476T>G
XM_011535204.1:c.-86T>G	XP_011533506.1:n.-86T>G
XM_011535205.1:c.-86T>G	XP_011533507.1:n.-86T>G
NM_000059.4:c.-86T>G MANE Select	NP_000050.3:n.-86T>G