LDH info

Canonical Allele Identifier: CA13577777
Gene: CCND2 HGNC NCBI
CCND2-AS1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 678294
ClinVar RCV Id: RCV000837873
dbSNP Id: rs1049606

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4273870C>T , CM000674.2:g.4273870C>T GRCh38
NC_000012.11:g.4383036C>T , CM000674.1:g.4383036C>T GRCh37
NC_000012.10:g.4253297C>T NCBI36
NG_034254.1:g.5135C>T

Transcript Alleles

HGVS Amino-acid change
NM_001759.3:c.-171C>T (CCND2) VV NP_001750.1:p.=
NR_125790.1:n.126+2189G>A (CCND2-AS1)
XM_005253813.3:c.-171C>T (CCND2) XP_005253870.1:p.=
NR_149145.1:n.182+1426G>A (CCND2-AS1)
NR_149146.1:n.182+1426G>A (CCND2-AS1)
NM_001759.4:c.-171C>T (CCND2) VV NP_001750.1:p.=
ENST00000261254.7:c.-171C>T ENSP00000261254.3:p.=