LDH info

Canonical Allele Identifier: CA387759830
Gene: BRCA2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 495095
ClinVar RCV Id: RCV000585687

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.32330918G>T , CM000675.2:g.32330918G>T GRCh38
NC_000013.10:g.32905055G>T , CM000675.1:g.32905055G>T GRCh37
NC_000013.9:g.31803055G>T NCBI36
NG_012772.3:g.20439G>T , LRG_293:g.20439G>T

Transcript Alleles

HGVS Amino-acid change
NM_000059.3:c.682-1G>T , LRG_293t1:c.682-1G>T NP_000050.2:p.=
XM_011535203.1:c.682-1G>T XP_011533505.1:p.=
XM_011535204.1:c.682-1G>T XP_011533506.1:p.=
XM_011535205.1:c.682-1G>T XP_011533507.1:p.=
ENST00000380152.7:c.682-1G>T ENSP00000369497.3:p.=
ENST00000530893.6:n.880-1G>T
ENST00000544455.5:c.682-1G>T ENSP00000439902.1:p.=
ENST00000614259.1:n.682-1G>T