Canonical Allele Identifier: CA387761775

Gene: BRCA2

Linked Data

• dbSNP Id: rs2137654419
• MyVariant Identifiers: chr13:g.32969044T>C (hg19) ; chr13:g.32394907T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32394907T>C , CM000675.2:g.32394907T>C	GRCh38
NC_000013.10:g.32969044T>C , CM000675.1:g.32969044T>C	GRCh37
NC_000013.9:g.31867044T>C	NCBI36
NG_012772.3:g.84428T>C , LRG_293:g.84428T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.9475T>C	ENSP00000434898.2:p.Phe3159Leu
ENST00000528762.2:c.*842T>C	ENSP00000433168.2:n.*842T>C
ENST00000530893.7:c.9106T>C	ENSP00000499438.2:p.Phe3036Leu
ENST00000665585.2:c.*1037T>C	ENSP00000499570.2:n.*1037T>C
ENST00000666593.2:c.*320T>C	ENSP00000499256.2:n.*320T>C
ENST00000700202.2:c.9424T>C	ENSP00000514856.2:p.Phe3142Leu
ENST00000700202.1:c.1891T>C	ENSP00000514856.1:p.Phe631Leu
ENST00000700203.1:n.1602T>C
ENST00000380152.8:c.9475T>C MANE Select	ENSP00000369497.3:p.Phe3159Leu
ENST00000544455.6:c.9475T>C	ENSP00000439902.1:p.Phe3159Leu
ENST00000614259.2:c.9483T>C	ENSP00000506251.1:n.9483T>C
ENST00000665585.1:c.2353T>C
ENST00000666593.1:c.497T>C	ENSP00000499256.1:n.497T>C
ENST00000680887.1:c.9475T>C	ENSP00000505508.1:p.Phe3159Leu
ENST00000380152.7:c.9475T>C	ENSP00000369497.3:p.Phe3159Leu
ENST00000470094.1:c.432T>C
ENST00000544455.5:c.9475T>C	ENSP00000439902.1:p.Phe3159Leu
NM_000059.3:c.9475T>C , LRG_293t1:c.9475T>C	NP_000050.2:p.Phe3159Leu
XM_011535203.1:c.9475T>C	XP_011533505.1:p.Phe3159Leu
XM_011535204.1:c.9379T>C	XP_011533506.1:p.Phe3127Leu
NM_000059.4:c.9475T>C MANE Select	NP_000050.3:p.Phe3159Leu