LDH info

Canonical Allele Identifier: CA025263
Gene: BRCA2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 52403
ClinVar RCV Id: RCV000257570
dbSNP Id: rs75096777

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32331012del , CM000675.2:g.32331012del GRCh38
NC_000013.10:g.32905149del , CM000675.1:g.32905149del GRCh37
NC_000013.9:g.31803149del NCBI36
NG_012772.3:g.20533del , LRG_293:g.20533del

Transcript Alleles

HGVS Amino-acid change
NM_000059.3:c.775del , LRG_293t1:c.775del NP_000050.2:p.Arg259GlufsTer18
XM_011535203.1:c.775del XP_011533505.1:p.Arg259GlufsTer18
XM_011535204.1:c.775del XP_011533506.1:p.Arg259GlufsTer18
XM_011535205.1:c.775del XP_011533507.1:p.Arg259GlufsTer18
ENST00000380152.7:c.775del ENSP00000369497.3:p.Arg259GlufsTer18
ENST00000530893.6:n.973del
ENST00000544455.5:c.775del ENSP00000439902.1:p.Arg259GlufsTer18
ENST00000614259.1:n.775del