LDH info

Canonical Allele Identifier: CA012133
Gene: MYH7 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14100
ClinVar RCV Id: RCV000015156
dbSNP Id: rs121913634

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23425372T>C , CM000676.2:g.23425372T>C GRCh38
NC_000014.8:g.23894581T>C , CM000676.1:g.23894581T>C GRCh37
NC_000014.7:g.22964421T>C NCBI36
NG_007884.1:g.15290A>G , LRG_384:g.15290A>G

Transcript Alleles

HGVS Amino-acid change
NM_000257.3:c.2333A>G VV NP_000248.2:p.Asp778Gly
XR_245686.3:n.2439A>G
XM_017021340.1:c.2333A>G XP_016876829.1:p.Asp778Gly
NM_000257.4:c.2333A>G VV MANE Preferred NP_000248.2:p.Asp778Gly
ENST00000355349.3:c.2333A>G ENSP00000347507.3:p.Asp778Gly