Canonical Allele Identifier: CA025405

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 185168
• ClinVar RCV Id: RCV000164537 ; RCV001207806 ; RCV001800483
• dbSNP Id: rs786201976
• gnomAD v4: 13-32363213-G-T
• MyVariant Identifiers: chr13:g.32937350G>T (hg19) ; chr13:g.32363213G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32363213G>T , CM000675.2:g.32363213G>T	GRCh38
NC_000013.10:g.32937350G>T , CM000675.1:g.32937350G>T	GRCh37
NC_000013.9:g.31835350G>T	NCBI36
NG_012772.3:g.52734G>T , LRG_293:g.52734G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.8011G>T	ENSP00000434898.2:p.Ala2671Ser
ENST00000528762.2:c.8011G>T	ENSP00000433168.2:p.Ala2671Ser
ENST00000530893.7:c.7642G>T	ENSP00000499438.2:p.Ala2548Ser
ENST00000665585.2:c.8011G>T	ENSP00000499570.2:p.Ala2671Ser
ENST00000666593.2:c.8011G>T	ENSP00000499256.2:p.Ala2671Ser
ENST00000700202.2:c.8011G>T	ENSP00000514856.2:p.Ala2671Ser
ENST00000700202.1:c.478G>T	ENSP00000514856.1:p.Ala160Ser
ENST00000380152.8:c.8011G>T MANE Select	ENSP00000369497.3:p.Ala2671Ser
ENST00000544455.6:c.8011G>T	ENSP00000439902.1:p.Ala2671Ser
ENST00000614259.2:c.8019G>T	ENSP00000506251.1:n.8019G>T
ENST00000665585.1:c.576G>T
ENST00000680887.1:c.8011G>T	ENSP00000505508.1:p.Ala2671Ser
ENST00000380152.7:c.8011G>T	ENSP00000369497.3:p.Ala2671Ser
ENST00000544455.5:c.8011G>T	ENSP00000439902.1:p.Ala2671Ser
NM_000059.3:c.8011G>T , LRG_293t1:c.8011G>T	NP_000050.2:p.Ala2671Ser
XM_011535203.1:c.8011G>T	XP_011533505.1:p.Ala2671Ser
XM_011535204.1:c.7915G>T	XP_011533506.1:p.Ala2639Ser
XM_011535205.1:c.8011G>T	XP_011533507.1:p.Ala2671Ser
NM_000059.4:c.8011G>T MANE Select	NP_000050.3:p.Ala2671Ser