LDH info

Canonical Allele Identifier: CA9556294
Gene: FUT2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 225366
ClinVar RCV Id: RCV000490450
dbSNP Id: rs1800028

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48703560C>T , CM000681.2:g.48703560C>T GRCh38
NC_000019.9:g.49206817C>T , CM000681.1:g.49206817C>T GRCh37
NC_000019.8:g.53898629C>T NCBI36
NG_007511.1:g.12590C>T

Transcript Alleles

HGVS Amino-acid change
NM_000511.5:c.604C>T VV NP_000502.4:p.Arg202Ter
NM_001097638.2:c.604C>T VV NP_001091107.1:p.Arg202Ter
NR_131188.1:n.289G>A
NM_000511.6:c.604C>T VV MANE Preferred NP_000502.4:p.Arg202Ter
NM_001097638.3:c.604C>T VV NP_001091107.1:p.Arg202Ter
ENST00000391876.5:c.604C>T ENSP00000375748.4:p.Arg202Ter
ENST00000425340.2:c.604C>T ENSP00000387498.2:p.Arg202Ter
ENST00000522966.1:c.604C>T ENSP00000430227.1:p.Arg202Ter