Canonical Allele Identifier: CA025677

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 38164
• ClinVar RCV Id: RCV002221480 ; RCV003162283 ; RCV003473221
• dbSNP Id: rs397507404
• gnomAD v4: 13-32370955-G-A
• MyVariant Identifiers: chr13:g.32945092G>A (hg19) ; chr13:g.32370955G>A (hg38)
• PubMed: PMID:12065746 ; PMID:22632462 ; PMID:24301060 ; PMID:24607278 ; PMID:25382762 ; PMID:25525159 ; PMID:26834852

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32370955G>A , CM000675.2:g.32370955G>A	GRCh38
NC_000013.10:g.32945092G>A , CM000675.1:g.32945092G>A	GRCh37
NC_000013.9:g.31843092G>A	NCBI36
NG_012772.3:g.60476G>A , LRG_293:g.60476G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.8488-1G>A	ENSP00000434898.2:n.8488-1G>A
ENST00000528762.2:c.8488-1G>A	ENSP00000433168.2:n.8488-1G>A
ENST00000530893.7:c.8119-1G>A	ENSP00000499438.2:n.8119-1G>A
ENST00000665585.2:c.8488-1G>A	ENSP00000499570.2:n.8488-1G>A
ENST00000666593.2:c.8488-1G>A	ENSP00000499256.2:n.8488-1G>A
ENST00000700202.2:c.8488-1G>A	ENSP00000514856.2:n.8488-1G>A
ENST00000700202.1:c.955-1G>A	ENSP00000514856.1:n.955-1G>A
ENST00000380152.8:c.8488-1G>A MANE Select	ENSP00000369497.3:n.8488-1G>A
ENST00000544455.6:c.8488-1G>A	ENSP00000439902.1:n.8488-1G>A
ENST00000614259.2:c.8496-1G>A	ENSP00000506251.1:n.8496-1G>A
ENST00000665585.1:c.1053-1G>A
ENST00000680887.1:c.8488-1G>A	ENSP00000505508.1:n.8488-1G>A
ENST00000380152.7:c.8488-1G>A	ENSP00000369497.3:n.8488-1G>A
ENST00000544455.5:c.8488-1G>A	ENSP00000439902.1:n.8488-1G>A
NM_000059.3:c.8488-1G>A , LRG_293t1:c.8488-1G>A	NP_000050.2:n.8488-1G>A
XM_011535203.1:c.8488-1G>A	XP_011533505.1:n.8488-1G>A
XM_011535204.1:c.8392-1G>A	XP_011533506.1:n.8392-1G>A
XM_011535205.1:c.8488-1G>A	XP_011533507.1:n.8488-1G>A
NM_000059.4:c.8488-1G>A MANE Select	NP_000050.3:n.8488-1G>A