Canonical Allele Identifier: CA247478039
Gene: BRCA2 HGNC NCBI

Linked Data

dbSNP Id: rs1050657422

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32315499C>T , CM000675.2:g.32315499C>T GRCh38
NC_000013.10:g.32889636C>T , CM000675.1:g.32889636C>T GRCh37
NC_000013.9:g.31787636C>T NCBI36
NG_012772.3:g.5020C>T , LRG_293:g.5020C>T
NG_017006.1:g.1456G>A
NG_017006.2:g.4865G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000544455.6:c.-40+354C>T ENSP00000439902.1:n.-40+354C>T
ENST00000380152.7:c.-208C>T ENSP00000369497.3:n.-208C>T
ENST00000544455.5:c.-208C>T ENSP00000439902.1:n.-208C>T
NM_000059.3:c.-208C>T , LRG_293t1:c.-208C>T NP_000050.2:n.-208C>T
XM_011535203.1:c.-40+354C>T XP_011533505.1:n.-40+354C>T
XM_011535204.1:c.-208C>T XP_011533506.1:n.-208C>T
XM_011535205.1:c.-208C>T XP_011533507.1:n.-208C>T