Canonical Allele Identifier: CA387757802

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 851261
• ClinVar RCV Id: RCV001055619 ; RCV002348413 ; RCV001090207
• dbSNP Id: rs1214427273
• gnomAD v4: 13-32326508-A-T
• MyVariant Identifiers: chr13:g.32900645A>T (hg19) ; chr13:g.32326508A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32326508A>T , CM000675.2:g.32326508A>T	GRCh38
NC_000013.10:g.32900645A>T , CM000675.1:g.32900645A>T	GRCh37
NC_000013.9:g.31798645A>T	NCBI36
NG_012772.3:g.16029A>T , LRG_293:g.16029A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.526A>T	ENSP00000434898.2:p.Thr176Ser
ENST00000528762.2:c.526A>T	ENSP00000433168.2:p.Thr176Ser
ENST00000530893.7:c.157A>T	ENSP00000499438.2:p.Thr53Ser
ENST00000665585.2:c.526A>T	ENSP00000499570.2:p.Thr176Ser
ENST00000666593.2:c.526A>T	ENSP00000499256.2:p.Thr176Ser
ENST00000700202.2:c.526A>T	ENSP00000514856.2:p.Thr176Ser
ENST00000700200.1:n.397A>T
ENST00000700201.1:c.*305A>T	ENSP00000514855.1:n.*305A>T
ENST00000380152.8:c.526A>T MANE Select	ENSP00000369497.3:p.Thr176Ser
ENST00000544455.6:c.526A>T	ENSP00000439902.1:p.Thr176Ser
ENST00000614259.2:c.526A>T	ENSP00000506251.1:p.Thr176Ser
ENST00000680887.1:c.526A>T	ENSP00000505508.1:p.Thr176Ser
ENST00000380152.7:c.526A>T	ENSP00000369497.3:p.Thr176Ser
ENST00000530893.6:n.724A>T
ENST00000544455.5:c.526A>T	ENSP00000439902.1:p.Thr176Ser
ENST00000614259.1:n.526A>T
NM_000059.3:c.526A>T , LRG_293t1:c.526A>T	NP_000050.2:p.Thr176Ser
XM_011535203.1:c.526A>T	XP_011533505.1:p.Thr176Ser
XM_011535204.1:c.526A>T	XP_011533506.1:p.Thr176Ser
XM_011535205.1:c.526A>T	XP_011533507.1:p.Thr176Ser
NM_000059.4:c.526A>T MANE Select	NP_000050.3:p.Thr176Ser