LDH info

Canonical Allele Identifier: CA216911
Gene: KRT14 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 14628
dbSNP Id: rs60171927

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586467T>C , CM000679.2:g.41586467T>C GRCh38
NC_000017.10:g.39742719T>C , CM000679.1:g.39742719T>C GRCh37
NC_000017.9:g.36996245T>C NCBI36
NG_008624.1:g.5429A>G

Transcript Alleles

HGVS Amino-acid change
NM_000526.4:c.368A>G VV NP_000517.2:p.Asn123Ser
NM_000526.5:c.368A>G VV MANE Preferred NP_000517.3:p.Asn123Ser
ENST00000167586.6:c.368A>G ENSP00000167586.6:p.Asn123Ser