Canonical Allele Identifier: CA697347903

Gene: BRCA2

Linked Data

• dbSNP Id: rs1448369360
• gnomAD v3: 13-32376232-C-T
• gnomAD v4: 13-32376232-C-T
• MyVariant Identifiers: chr13:g.32950369C>T (hg19) ; chr13:g.32376232C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376232C>T , CM000675.2:g.32376232C>T	GRCh38
NC_000013.10:g.32950369C>T , CM000675.1:g.32950369C>T	GRCh37
NC_000013.9:g.31848369C>T	NCBI36
NG_012772.3:g.65753C>T , LRG_293:g.65753C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8633-438C>T	ENSP00000434898.2:n.8633-438C>T
ENST00000528762.2:c.8697-438C>T	ENSP00000433168.2:n.8697-438C>T
ENST00000530893.7:c.8264-438C>T	ENSP00000499438.2:n.8264-438C>T
ENST00000665585.2:c.*195-438C>T	ENSP00000499570.2:n.*195-438C>T
ENST00000666593.2:c.8633-438C>T	ENSP00000499256.2:n.8633-438C>T
ENST00000700202.2:c.8633-438C>T	ENSP00000514856.2:n.8633-438C>T
ENST00000700202.1:c.1100-438C>T	ENSP00000514856.1:n.1100-438C>T
ENST00000700203.1:n.322C>T
ENST00000380152.8:c.8633-438C>T MANE Select	ENSP00000369497.3:n.8633-438C>T
ENST00000544455.6:c.8633-438C>T	ENSP00000439902.1:n.8633-438C>T
ENST00000614259.2:c.8641-438C>T	ENSP00000506251.1:n.8641-438C>T
ENST00000665585.1:c.1511-438C>T
ENST00000680887.1:c.8633-438C>T	ENSP00000505508.1:n.8633-438C>T
ENST00000380152.7:c.8633-438C>T	ENSP00000369497.3:n.8633-438C>T
ENST00000528762.1:c.195-438C>T	ENSP00000433168.1:n.195-438C>T
ENST00000544455.5:c.8633-438C>T	ENSP00000439902.1:n.8633-438C>T
NM_000059.3:c.8633-438C>T , LRG_293t1:c.8633-438C>T	NP_000050.2:n.8633-438C>T
XM_011535203.1:c.8633-438C>T	XP_011533505.1:n.8633-438C>T
XM_011535204.1:c.8537-438C>T	XP_011533506.1:n.8537-438C>T
XM_011535205.1:c.8633-438C>T	XP_011533507.1:n.8633-438C>T
NM_000059.4:c.8633-438C>T MANE Select	NP_000050.3:n.8633-438C>T