LDH info

Canonical Allele Identifier: CA127784
Gene: AGT HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 18068
dbSNP Id: rs699

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230710048A>G , CM000663.2:g.230710048A>G GRCh38
NC_000001.10:g.230845794A>G , CM000663.1:g.230845794A>G GRCh37
NC_000001.9:g.228912417A>G NCBI36
NG_008836.1:g.9543T>C
NG_008836.2:g.9543T>C

Transcript Alleles

HGVS Amino-acid change
NM_000029.3:c.803T>C VV NP_000020.1:p.Met268Thr
NM_000029.4:c.803T>C VV MANE Preferred NP_000020.1:p.Met268Thr
ENST00000366667.4:c.803T>C ENSP00000355627.4:p.Met268Thr