Canonical Allele Identifier: CA387767736

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137665833
• MyVariant Identifiers: chr13:g.32972671G>T (hg19) ; chr13:g.32398534G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32398534G>T , CM000675.2:g.32398534G>T	GRCh38
NC_000013.10:g.32972671G>T , CM000675.1:g.32972671G>T	GRCh37
NC_000013.9:g.31870671G>T	NCBI36
NG_012772.3:g.88055G>T , LRG_293:g.88055G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.*544G>T	ENSP00000434898.2:n.*544G>T
ENST00000528762.2:c.*1388G>T	ENSP00000433168.2:n.*1388G>T
ENST00000530893.7:c.9652G>T	ENSP00000499438.2:p.Asp3218Tyr
ENST00000665585.2:c.*1583G>T	ENSP00000499570.2:n.*1583G>T
ENST00000700202.2:c.9970G>T	ENSP00000514856.2:p.Asp3324Tyr
ENST00000700202.1:c.2437G>T	ENSP00000514856.1:p.Asp813Tyr
ENST00000700203.1:n.2148G>T
ENST00000380152.8:c.10021G>T MANE Select	ENSP00000369497.3:p.Asp3341Tyr
ENST00000544455.6:c.10021G>T	ENSP00000439902.1:p.Asp3341Tyr
ENST00000614259.2:c.10029G>T	ENSP00000506251.1:n.10029G>T
ENST00000680887.1:c.10021G>T	ENSP00000505508.1:p.Asp3341Tyr
ENST00000380152.7:c.10021G>T	ENSP00000369497.3:p.Asp3341Tyr
ENST00000544455.5:c.10021G>T	ENSP00000439902.1:p.Asp3341Tyr
NM_000059.3:c.10021G>T , LRG_293t1:c.10021G>T	NP_000050.2:p.Asp3341Tyr
XM_011535203.1:c.10021G>T	XP_011533505.1:p.Asp3341Tyr
XM_011535204.1:c.9925G>T	XP_011533506.1:p.Asp3309Tyr
NM_000059.4:c.10021G>T MANE Select	NP_000050.3:p.Asp3341Tyr