Canonical Allele Identifier: CA387760741

Gene: BRCA2

Linked Data

• dbSNP Id: rs1555289499
• MyVariant Identifiers: chr13:g.32968835C>A (hg19) ; chr13:g.32394698C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32394698C>A , CM000675.2:g.32394698C>A	GRCh38
NC_000013.10:g.32968835C>A , CM000675.1:g.32968835C>A	GRCh37
NC_000013.9:g.31866835C>A	NCBI36
NG_012772.3:g.84219C>A , LRG_293:g.84219C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.9266C>A	ENSP00000434898.2:p.Pro3089His
ENST00000528762.2:c.*633C>A	ENSP00000433168.2:n.*633C>A
ENST00000530893.7:c.8897C>A	ENSP00000499438.2:p.Pro2966His
ENST00000665585.2:c.*828C>A	ENSP00000499570.2:n.*828C>A
ENST00000666593.2:c.*111C>A	ENSP00000499256.2:n.*111C>A
ENST00000700202.2:c.9215C>A	ENSP00000514856.2:p.Pro3072His
ENST00000700202.1:c.1682C>A	ENSP00000514856.1:p.Pro561His
ENST00000700203.1:n.1393C>A
ENST00000380152.8:c.9266C>A MANE Select	ENSP00000369497.3:p.Pro3089His
ENST00000544455.6:c.9266C>A	ENSP00000439902.1:p.Pro3089His
ENST00000614259.2:c.9274C>A	ENSP00000506251.1:n.9274C>A
ENST00000665585.1:c.2144C>A
ENST00000666593.1:c.288C>A	ENSP00000499256.1:n.288C>A
ENST00000680887.1:c.9266C>A	ENSP00000505508.1:p.Pro3089His
ENST00000380152.7:c.9266C>A	ENSP00000369497.3:p.Pro3089His
ENST00000470094.1:c.223C>A
ENST00000544455.5:c.9266C>A	ENSP00000439902.1:p.Pro3089His
NM_000059.3:c.9266C>A , LRG_293t1:c.9266C>A	NP_000050.2:p.Pro3089His
XM_011535203.1:c.9266C>A	XP_011533505.1:p.Pro3089His
XM_011535204.1:c.9170C>A	XP_011533506.1:p.Pro3057His
NM_000059.4:c.9266C>A MANE Select	NP_000050.3:p.Pro3089His