Canonical Allele Identifier: CA2622596971
Gene: BRCA2 HGNC NCBI

Linked Data

dbSNP Id: rs2138694742

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32315477C>A , CM000675.2:g.32315477C>A GRCh38
NC_000013.10:g.32889614C>A , CM000675.1:g.32889614C>A GRCh37
NC_000013.9:g.31787614C>A NCBI36
NG_012772.3:g.4998C>A , LRG_293:g.4998C>A
NG_017006.1:g.1478G>T
NG_017006.2:g.4887G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000544455.6:c.-40+332C>A ENSP00000439902.1:n.-40+332C>A
ENST00000380152.7:c.-230C>A ENSP00000369497.3:n.-230C>A
XM_011535203.1:c.-40+332C>A XP_011533505.1:n.-40+332C>A
XM_011535204.1:c.-230C>A XP_011533506.1:n.-230C>A
XM_011535205.1:c.-230C>A XP_011533507.1:n.-230C>A