LDH info

Canonical Allele Identifier: CA387760214
Gene: BRCA2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 491334
ClinVar RCV Id: RCV000581375

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32331018G>A , CM000675.2:g.32331018G>A GRCh38
NC_000013.10:g.32905155G>A , CM000675.1:g.32905155G>A GRCh37
NC_000013.9:g.31803155G>A NCBI36
NG_012772.3:g.20539G>A , LRG_293:g.20539G>A

Transcript Alleles

HGVS Amino-acid change
NM_000059.3:c.781G>A , LRG_293t1:c.781G>A NP_000050.2:p.Ala261Thr
XM_011535203.1:c.781G>A XP_011533505.1:p.Ala261Thr
XM_011535204.1:c.781G>A XP_011533506.1:p.Ala261Thr
XM_011535205.1:c.781G>A XP_011533507.1:p.Ala261Thr
ENST00000380152.7:c.781G>A ENSP00000369497.3:p.Ala261Thr
ENST00000530893.6:n.979G>A
ENST00000544455.5:c.781G>A ENSP00000439902.1:p.Ala261Thr
ENST00000614259.1:n.781G>A