Canonical Allele Identifier: CA025377

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 52458
• ClinVar RCV Id: RCV000077420 ; RCV000480484 ; RCV000773273 ; RCV001386986
• dbSNP Id: rs80359029
• gnomAD v4: 13-32363180-T-G
• MyVariant Identifiers: chr13:g.32937317T>G (hg19) ; chr13:g.32363180T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32363180T>G , CM000675.2:g.32363180T>G	GRCh38
NC_000013.10:g.32937317T>G , CM000675.1:g.32937317T>G	GRCh37
NC_000013.9:g.31835317T>G	NCBI36
NG_012772.3:g.52701T>G , LRG_293:g.52701T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7978T>G	ENSP00000434898.2:p.Tyr2660Asp
ENST00000528762.2:c.7978T>G	ENSP00000433168.2:p.Tyr2660Asp
ENST00000530893.7:c.7609T>G	ENSP00000499438.2:p.Tyr2537Asp
ENST00000665585.2:c.7978T>G	ENSP00000499570.2:p.Tyr2660Asp
ENST00000666593.2:c.7978T>G	ENSP00000499256.2:p.Tyr2660Asp
ENST00000700202.2:c.7978T>G	ENSP00000514856.2:p.Tyr2660Asp
ENST00000700202.1:c.445T>G	ENSP00000514856.1:p.Tyr149Asp
ENST00000380152.8:c.7978T>G MANE Select	ENSP00000369497.3:p.Tyr2660Asp
ENST00000544455.6:c.7978T>G	ENSP00000439902.1:p.Tyr2660Asp
ENST00000614259.2:c.7986T>G	ENSP00000506251.1:n.7986T>G
ENST00000665585.1:c.543T>G
ENST00000680887.1:c.7978T>G	ENSP00000505508.1:p.Tyr2660Asp
ENST00000380152.7:c.7978T>G	ENSP00000369497.3:p.Tyr2660Asp
ENST00000544455.5:c.7978T>G	ENSP00000439902.1:p.Tyr2660Asp
NM_000059.3:c.7978T>G , LRG_293t1:c.7978T>G	NP_000050.2:p.Tyr2660Asp
XM_011535203.1:c.7978T>G	XP_011533505.1:p.Tyr2660Asp
XM_011535204.1:c.7882T>G	XP_011533506.1:p.Tyr2628Asp
XM_011535205.1:c.7978T>G	XP_011533507.1:p.Tyr2660Asp
NM_000059.4:c.7978T>G MANE Select	NP_000050.3:p.Tyr2660Asp