Canonical Allele Identifier: CA025112

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 52342
• ClinVar RCV Id: RCV000077402 ; RCV000162811 ; RCV000478977 ; RCV000657023 ; RCV000779955 ; RCV001080469
• dbSNP Id: rs80358974
• gnomAD v2: 13-32930613-T-C
• gnomAD v3: 13-32356476-T-C
• gnomAD v4: 13-32356476-T-C
• MyVariant Identifiers: chr13:g.32930613T>C (hg19) ; chr13:g.32356476T>C (hg38)
• PubMed: PMID:10923033

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32356476T>C , CM000675.2:g.32356476T>C	GRCh38
NC_000013.10:g.32930613T>C , CM000675.1:g.32930613T>C	GRCh37
NC_000013.9:g.31828613T>C	NCBI36
NG_012772.3:g.45997T>C , LRG_293:g.45997T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.7484T>C	ENSP00000434898.2:p.Ile2495Thr
ENST00000528762.2:c.7484T>C	ENSP00000433168.2:p.Ile2495Thr
ENST00000530893.7:c.7115T>C	ENSP00000499438.2:p.Ile2372Thr
ENST00000665585.2:c.7484T>C	ENSP00000499570.2:p.Ile2495Thr
ENST00000666593.2:c.7484T>C	ENSP00000499256.2:p.Ile2495Thr
ENST00000700202.2:c.7484T>C	ENSP00000514856.2:p.Ile2495Thr
ENST00000380152.8:c.7484T>C MANE Select	ENSP00000369497.3:p.Ile2495Thr
ENST00000544455.6:c.7484T>C	ENSP00000439902.1:p.Ile2495Thr
ENST00000614259.2:c.7484T>C	ENSP00000506251.1:p.Ile2495Thr
ENST00000665585.1:c.49T>C
ENST00000680887.1:c.7484T>C	ENSP00000505508.1:p.Ile2495Thr
ENST00000380152.7:c.7484T>C	ENSP00000369497.3:p.Ile2495Thr
ENST00000544455.5:c.7484T>C	ENSP00000439902.1:p.Ile2495Thr
ENST00000614259.1:n.7484T>C
NM_000059.3:c.7484T>C , LRG_293t1:c.7484T>C	NP_000050.2:p.Ile2495Thr
XM_011535203.1:c.7484T>C	XP_011533505.1:p.Ile2495Thr
XM_011535204.1:c.7388T>C	XP_011533506.1:p.Ile2463Thr
XM_011535205.1:c.7484T>C	XP_011533507.1:p.Ile2495Thr
NM_000059.4:c.7484T>C MANE Select	NP_000050.3:p.Ile2495Thr