Canonical Allele Identifier: CA387788967

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 495480
• ClinVar RCV Id: RCV000589502 ; RCV000773071 ; RCV001853971
• dbSNP Id: rs1405631299
• gnomAD v2: 13-32914760-C-T
• gnomAD v3: 13-32340623-C-T
• gnomAD v4: 13-32340623-C-T
• MyVariant Identifiers: chr13:g.32914760C>T (hg19) ; chr13:g.32340623C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32340623C>T , CM000675.2:g.32340623C>T	GRCh38
NC_000013.10:g.32914760C>T , CM000675.1:g.32914760C>T	GRCh37
NC_000013.9:g.31812760C>T	NCBI36
NG_012772.3:g.30144C>T , LRG_293:g.30144C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.6268C>T	ENSP00000434898.2:p.His2090Tyr
ENST00000528762.2:c.6268C>T	ENSP00000433168.2:p.His2090Tyr
ENST00000530893.7:c.5899C>T	ENSP00000499438.2:p.His1967Tyr
ENST00000665585.2:c.6268C>T	ENSP00000499570.2:p.His2090Tyr
ENST00000666593.2:c.6268C>T	ENSP00000499256.2:p.His2090Tyr
ENST00000700202.2:c.6268C>T	ENSP00000514856.2:p.His2090Tyr
ENST00000380152.8:c.6268C>T MANE Select	ENSP00000369497.3:p.His2090Tyr
ENST00000544455.6:c.6268C>T	ENSP00000439902.1:p.His2090Tyr
ENST00000614259.2:c.6268C>T	ENSP00000506251.1:p.His2090Tyr
ENST00000680887.1:c.6268C>T	ENSP00000505508.1:p.His2090Tyr
ENST00000380152.7:c.6268C>T	ENSP00000369497.3:p.His2090Tyr
ENST00000544455.5:c.6268C>T	ENSP00000439902.1:p.His2090Tyr
ENST00000614259.1:n.6268C>T
NM_000059.3:c.6268C>T , LRG_293t1:c.6268C>T	NP_000050.2:p.His2090Tyr
XM_011535203.1:c.6268C>T	XP_011533505.1:p.His2090Tyr
XM_011535204.1:c.6268C>T	XP_011533506.1:p.His2090Tyr
XM_011535205.1:c.6268C>T	XP_011533507.1:p.His2090Tyr
NM_000059.4:c.6268C>T MANE Select	NP_000050.3:p.His2090Tyr