Canonical Allele Identifier: CA2727841621

Gene: BRCA2

Linked Data

• dbSNP Id: rs886050116

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32399186G>C , CM000675.2:g.32399186G>C	GRCh38
NC_000013.10:g.32973323G>C , CM000675.1:g.32973323G>C	GRCh37
NC_000013.9:g.31871323G>C	NCBI36
NG_012772.3:g.88707G>C , LRG_293:g.88707G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.*1196G>C	ENSP00000434898.2:n.*1196G>C
ENST00000530893.7:c.*416G>C	ENSP00000499438.2:n.*416G>C
ENST00000380152.8:c.*416G>C MANE Select	ENSP00000369497.3:n.*416G>C
ENST00000544455.6:c.*416G>C	ENSP00000439902.1:n.*416G>C
ENST00000614259.2:c.10681G>C	ENSP00000506251.1:n.10681G>C
ENST00000680887.1:c.*416G>C	ENSP00000505508.1:n.*416G>C
ENST00000380152.7:c.*416G>C	ENSP00000369497.3:n.*416G>C
ENST00000544455.5:c.*416G>C	ENSP00000439902.1:n.*416G>C
NM_000059.3:c.*416G>C , LRG_293t1:c.*416G>C	NP_000050.2:n.*416G>C
XM_011535203.1:c.*416G>C	XP_011533505.1:n.*416G>C
XM_011535204.1:c.*416G>C	XP_011533506.1:n.*416G>C
NM_000059.4:c.*416G>C MANE Select	NP_000050.3:n.*416G>C