LDH info

Canonical Allele Identifier: CA1448217
Gene: AGT HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 429788
ClinVar RCV Id: RCV000493969
dbSNP Id: rs747815674

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230709994C>A , CM000663.2:g.230709994C>A GRCh38
NC_000001.10:g.230845740C>A , CM000663.1:g.230845740C>A GRCh37
NC_000001.9:g.228912363C>A NCBI36
NG_008836.1:g.9597G>T
NG_008836.2:g.9597G>T

Transcript Alleles

HGVS Amino-acid change
NM_000029.3:c.856+1G>T VV NP_000020.1:p.=
NM_000029.4:c.856+1G>T VV MANE Preferred NP_000020.1:p.=
ENST00000366667.4:c.856+1G>T ENSP00000355627.4:p.=