LDH info

Canonical Allele Identifier: CA15091002
Gene: HSPG2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2445142

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21899250G>C , CM000663.2:g.21899250G>C GRCh38
NC_000001.10:g.22225743G>C , CM000663.1:g.22225743G>C GRCh37
NC_000001.9:g.22098330G>C NCBI36
NG_016740.1:g.43008C>G

Transcript Alleles

HGVS Amino-acid change
NM_001291860.1:c.64-2940C>G VV NP_001278789.1:p.=
NM_005529.6:c.64-2940C>G VV NP_005520.4:p.=
XM_006710594.2:c.64-2940C>G XP_006710657.1:p.=
XM_006710595.2:c.64-2940C>G XP_006710658.1:p.=
XM_006710596.2:c.64-2940C>G XP_006710659.1:p.=
XM_006710597.2:c.64-2940C>G XP_006710660.1:p.=
XM_011541317.1:c.64-2940C>G XP_011539619.1:p.=
XM_011541318.1:c.64-2940C>G XP_011539620.1:p.=
XM_011541319.1:c.64-2940C>G XP_011539621.1:p.=
XM_011541320.1:c.64-2940C>G XP_011539622.1:p.=
XM_011541321.1:c.64-2940C>G XP_011539623.1:p.=
XM_011541322.1:c.64-2940C>G XP_011539624.1:p.=
XM_011541318.2:c.64-2940C>G XP_011539620.1:p.=
NM_005529.7:c.64-2940C>G VV MANE Preferred NP_005520.4:p.=
NM_001291860.2:c.64-2940C>G VV NP_001278789.1:p.=
ENST00000374695.7:c.64-2940C>G ENSP00000363827.3:p.=