Canonical Allele Identifier: CA387754847

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 1410376
• ClinVar RCV Id: RCV001916416
• dbSNP Id: rs2137612969
• MyVariant Identifiers: chr13:g.32950872G>T (hg19) ; chr13:g.32376735G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376735G>T , CM000675.2:g.32376735G>T	GRCh38
NC_000013.10:g.32950872G>T , CM000675.1:g.32950872G>T	GRCh37
NC_000013.9:g.31848872G>T	NCBI36
NG_012772.3:g.66256G>T , LRG_293:g.66256G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8698G>T	ENSP00000434898.2:p.Asp2900Tyr
ENST00000528762.2:c.*65G>T	ENSP00000433168.2:n.*65G>T
ENST00000530893.7:c.8329G>T	ENSP00000499438.2:p.Asp2777Tyr
ENST00000665585.2:c.*260G>T	ENSP00000499570.2:n.*260G>T
ENST00000666593.2:c.8698G>T	ENSP00000499256.2:p.Asp2900Tyr
ENST00000700202.2:c.8698G>T	ENSP00000514856.2:p.Asp2900Tyr
ENST00000700202.1:c.1165G>T	ENSP00000514856.1:p.Asp389Tyr
ENST00000700203.1:n.825G>T
ENST00000380152.8:c.8698G>T MANE Select	ENSP00000369497.3:p.Asp2900Tyr
ENST00000544455.6:c.8698G>T	ENSP00000439902.1:p.Asp2900Tyr
ENST00000614259.2:c.8706G>T	ENSP00000506251.1:n.8706G>T
ENST00000665585.1:c.1576G>T
ENST00000680887.1:c.8698G>T	ENSP00000505508.1:p.Asp2900Tyr
ENST00000380152.7:c.8698G>T	ENSP00000369497.3:p.Asp2900Tyr
ENST00000528762.1:c.260G>T	ENSP00000433168.1:n.260G>T
ENST00000544455.5:c.8698G>T	ENSP00000439902.1:p.Asp2900Tyr
NM_000059.3:c.8698G>T , LRG_293t1:c.8698G>T	NP_000050.2:p.Asp2900Tyr
XM_011535203.1:c.8698G>T	XP_011533505.1:p.Asp2900Tyr
XM_011535204.1:c.8602G>T	XP_011533506.1:p.Asp2868Tyr
XM_011535205.1:c.8698G>T	XP_011533507.1:p.Asp2900Tyr
NM_000059.4:c.8698G>T MANE Select	NP_000050.3:p.Asp2900Tyr