LDH info

Canonical Allele Identifier: CA5669525
Gene: CYP17A1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs104894150

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102834850A>C , CM000672.2:g.102834850A>C GRCh38
NC_000010.10:g.104594607A>C , CM000672.1:g.104594607A>C GRCh37
NC_000010.9:g.104584597A>C NCBI36
NG_007955.1:g.7684T>G

Transcript Alleles

HGVS Amino-acid change
NM_000102.3:c.601T>G VV NP_000093.1:p.Tyr201Asp
NM_000102.4:c.601T>G VV MANE Preferred NP_000093.1:p.Tyr201Asp
ENST00000369887.3:c.601T>G ENSP00000358903.3:p.Tyr201Asp
ENST00000489268.1:n.855T>G