Canonical Allele Identifier: CA2082772270
Gene: BRCA2 HGNC NCBI

Linked Data

dbSNP Id: rs2072244830
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32315459T>C , CM000675.2:g.32315459T>C GRCh38
NC_000013.10:g.32889596T>C , CM000675.1:g.32889596T>C GRCh37
NC_000013.9:g.31787596T>C NCBI36
NG_012772.3:g.4980T>C , LRG_293:g.4980T>C
NG_017006.1:g.1496A>G
NG_017006.2:g.4905A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000544455.6:c.-40+314T>C ENSP00000439902.1:n.-40+314T>C
XM_011535203.1:c.-40+314T>C XP_011533505.1:n.-40+314T>C
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