LDH info

Canonical Allele Identifier: CA15206502
Gene: MATN3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10178256

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19998305G>A , CM000664.2:g.19998305G>A GRCh38
NC_000002.11:g.20198066G>A , CM000664.1:g.20198066G>A GRCh37
NC_000002.10:g.20061547G>A NCBI36
NG_008087.1:g.19390C>T

Transcript Alleles

HGVS Amino-acid change
NM_002381.4:c.1169-1046C>T VV NP_002372.1:p.=
NR_110235.1:n.292-901G>A
NM_002381.5:c.1169-1046C>T VV MANE Preferred NP_002372.1:p.=
ENST00000407540.7:c.1169-1046C>T ENSP00000383894.3:p.=
ENST00000421259.2:c.1043-1046C>T ENSP00000398753.2:p.=