LDH info

Canonical Allele Identifier: CA30689391
Gene: NPR1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10082235

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153684174C>T , CM000663.2:g.153684174C>T GRCh38
NC_000001.10:g.153656650C>T , CM000663.1:g.153656650C>T GRCh37
NC_000001.9:g.151923274C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_000906.3:c.1484+350C>T VV NP_000897.3:p.=
XM_005245218.1:c.1484+350C>T XP_005245275.1:p.=
XM_006711342.1:c.1484+350C>T XP_006711405.1:p.=
XM_006711343.1:c.1484+350C>T XP_006711406.1:p.=
XM_011509585.1:c.1484+350C>T XP_011507887.1:p.=
XM_005245218.2:c.1484+350C>T XP_005245275.1:p.=
XM_017001374.2:c.1484+350C>T XP_016856863.1:p.=
NM_000906.4:c.1484+350C>T VV MANE Preferred NP_000897.3:p.=
ENST00000368680.3:c.1484+350C>T ENSP00000357669.3:p.=