LDH info

Canonical Allele Identifier: CA10623369
Gene: SH3TC2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 351718
dbSNP Id: rs753563756

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148994606G>A , CM000667.2:g.148994606G>A GRCh38
NC_000005.9:g.148374169G>A , CM000667.1:g.148374169G>A GRCh37
NC_000005.8:g.148354362G>A NCBI36
NG_007947.2:g.73569C>T , LRG_269:g.73569C>T

Transcript Alleles

HGVS Amino-acid change
NM_024577.3:c.*10105C>T , LRG_269t1:c.*10105C>T NP_078853.2:p.=
NM_024577.4:c.*10105C>T VV MANE Preferred NP_078853.2:p.=
ENST00000504690.5:c.*12+9120C>T ENSP00000425627.1:p.=
ENST00000510350.1:n.231+12275C>T