LDH info

Canonical Allele Identifier: CA125961
Gene: HBA1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 15856
dbSNP Id: rs35723200

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.177403T>C , CM000678.2:g.177403T>C GRCh38
NC_000016.9:g.227402T>C , CM000678.1:g.227402T>C GRCh37
NC_000016.8:g.167402T>C NCBI36
NG_000006.1:g.38266T>C
NG_059186.1:g.5753T>C

Transcript Alleles

HGVS Amino-acid change
NM_000558.4:c.421T>C VV NP_000549.1:p.Tyr141His
NM_000558.5:c.421T>C VV MANE Preferred NP_000549.1:p.Tyr141His
ENST00000320868.9:c.421T>C ENSP00000322421.5:p.Tyr141His
ENST00000397797.1:c.325T>C ENSP00000380899.1:p.Tyr109His
ENST00000472694.1:n.557T>C