Canonical Allele Identifier: CA6941180

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 1001575
• ClinVar RCV Id: RCV001297894
• dbSNP Id: rs757206472
• ExAC: 13:32937347 T / C
• gnomAD v2: 13-32937347-T-C
• gnomAD v4: 13-32363210-T-C
• MyVariant Identifiers: chr13:g.32937347T>C (hg19) ; chr13:g.32363210T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32363210T>C , CM000675.2:g.32363210T>C	GRCh38
NC_000013.10:g.32937347T>C , CM000675.1:g.32937347T>C	GRCh37
NC_000013.9:g.31835347T>C	NCBI36
NG_012772.3:g.52731T>C , LRG_293:g.52731T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000470094.2:c.8008T>C	ENSP00000434898.2:p.Ser2670Pro
ENST00000528762.2:c.8008T>C	ENSP00000433168.2:p.Ser2670Pro
ENST00000530893.7:c.7639T>C	ENSP00000499438.2:p.Ser2547Pro
ENST00000665585.2:c.8008T>C	ENSP00000499570.2:p.Ser2670Pro
ENST00000666593.2:c.8008T>C	ENSP00000499256.2:p.Ser2670Pro
ENST00000700202.2:c.8008T>C	ENSP00000514856.2:p.Ser2670Pro
ENST00000700202.1:c.475T>C	ENSP00000514856.1:p.Ser159Pro
ENST00000380152.8:c.8008T>C MANE Select	ENSP00000369497.3:p.Ser2670Pro
ENST00000544455.6:c.8008T>C	ENSP00000439902.1:p.Ser2670Pro
ENST00000614259.2:c.8016T>C	ENSP00000506251.1:n.8016T>C
ENST00000665585.1:c.573T>C
ENST00000680887.1:c.8008T>C	ENSP00000505508.1:p.Ser2670Pro
ENST00000380152.7:c.8008T>C	ENSP00000369497.3:p.Ser2670Pro
ENST00000544455.5:c.8008T>C	ENSP00000439902.1:p.Ser2670Pro
NM_000059.3:c.8008T>C , LRG_293t1:c.8008T>C	NP_000050.2:p.Ser2670Pro
XM_011535203.1:c.8008T>C	XP_011533505.1:p.Ser2670Pro
XM_011535204.1:c.7912T>C	XP_011533506.1:p.Ser2638Pro
XM_011535205.1:c.8008T>C	XP_011533507.1:p.Ser2670Pro
NM_000059.4:c.8008T>C MANE Select	NP_000050.3:p.Ser2670Pro