LDH info

Canonical Allele Identifier: CA16602268
Gene: HBA2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 375746
dbSNP Id: rs41474145

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.173009_173013del , CM000678.2:g.173009_173013del GRCh38
NC_000016.9:g.223008_223012del , CM000678.1:g.223008_223012del GRCh37
NC_000016.8:g.163008_163012del NCBI36
NG_000006.1:g.33872_33876del
NG_059186.1:g.1359_1363del
NG_059271.1:g.5163_5167del

Transcript Alleles

HGVS Amino-acid change
NM_000517.4:c.95+2_95+6del VV
NM_000517.6:c.95+2_95+6del VV MANE Preferred
ENST00000251595.10:c.95+2_95+6del
ENST00000397806.1:c.-2+51_-2+55del ENSP00000380908.1:p.=
ENST00000482565.1:n.116_120del
ENST00000484216.1:n.64+2_64+6del