LDH info

Canonical Allele Identifier: CA254037
Gene: MGAT2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 6990
ClinVar RCV Id: RCV000007406
dbSNP Id: rs104894447

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.49622053A>G , CM000676.2:g.49622053A>G GRCh38
NC_000014.8:g.50088771A>G , CM000676.1:g.50088771A>G GRCh37
NC_000014.7:g.49158521A>G NCBI36
NG_008920.1:g.6283A>G
NG_033054.1:g.3579T>C

Transcript Alleles

HGVS Amino-acid change
NM_002408.3:c.785A>G VV NP_002399.1:p.His262Arg
NM_002408.4:c.785A>G VV MANE Preferred NP_002399.1:p.His262Arg
ENST00000305386.3:c.785A>G ENSP00000307423.2:p.His262Arg