LDH info

Canonical Allele Identifier: CA14643263
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 39302
ClinVar RCV Id: RCV000032585
dbSNP Id: rs1800469

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41354391A>G , CM000681.2:g.41354391A>G GRCh38
NC_000019.9:g.41860296A>G , CM000681.1:g.41860296A>G GRCh37
NC_000019.8:g.46552136A>G NCBI36
NG_013091.1:g.14783T>C
NG_013364.1:g.4536T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000539627.5:c.-30+3189A>G ENSP00000441900.1:p.=
ENST00000604123.5:c.142+76A>G ENSP00000474871.1:p.=
ENST00000604424.1:n.350+3189A>G