LDH info

Canonical Allele Identifier: CA200766397
Gene: ABO HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 769757
ClinVar RCV Id: RCV000948820
dbSNP Id: rs512770
MyVariant Identifiers: chr9:g.133258116G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258116G>A , CM000671.2:g.133258116G>A GRCh38
NG_006669.1:g.19548C>T
NG_006669.2:g.22099C>T

Transcript Alleles

HGVS Amino-acid change
NM_020469.2:c.220C>T VV NP_065202.2:p.Pro74Ser
NM_020469.3:c.220C>T VV NP_065202.2:p.Pro74Ser
ENST00000453660.3:n.232C>T
ENST00000538324.2:c.220C>T ENSP00000483018.1:p.Pro74Ser
ENST00000611156.4:c.220C>T ENSP00000483265.1:p.Pro74Ser