LDH info

Canonical Allele Identifier: CA115071
Gene: WDR36 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 1580
dbSNP Id: rs34595252

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.111119021A>G , CM000667.2:g.111119021A>G GRCh38
NC_000005.9:g.110454719A>G , CM000667.1:g.110454719A>G GRCh37
NC_000005.8:g.110482618A>G NCBI36
NG_008979.1:g.31850A>G

Transcript Alleles

HGVS Amino-acid change
NM_139281.2:c.1973A>G VV NP_644810.1:p.Asp658Gly
XM_011543163.1:c.1973A>G XP_011541465.1:p.Asp658Gly
ENST00000506538.6:c.1973A>G ENSP00000423067.2:p.Asp658Gly
ENST00000513710.3:c.1805A>G ENSP00000424628.3:p.Asp602Gly
ENST00000612402.4:c.1973A>G ENSP00000479950.1:p.Asp658Gly