LDH info

Canonical Allele Identifier: CA10719600
Gene: RUNX3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs760805

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.24925432A>T , CM000663.2:g.24925432A>T GRCh38
NC_000001.10:g.25251923A>T , CM000663.1:g.25251923A>T GRCh37
NC_000001.9:g.25124510A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001031680.2:c.481+2142T>A VV NP_001026850.1:p.=
NM_004350.2:c.439+2142T>A VV NP_004341.1:p.=
XM_005246024.3:c.481+2142T>A XP_005246081.1:p.=
XM_011542351.1:c.481+2142T>A XP_011540653.1:p.=
NM_001320672.1:c.481+2142T>A VV NP_001307601.1:p.=
XM_005246024.4:c.481+2142T>A XP_005246081.1:p.=
XR_001737942.1:n.1104A>T
NM_004350.3:c.439+2142T>A VV MANE Preferred NP_004341.1:p.=
ENST00000308873.10:c.439+2142T>A ENSP00000308051.6:p.=
ENST00000338888.3:c.481+2142T>A ENSP00000343477.3:p.=
ENST00000399916.5:c.481+2142T>A ENSP00000382800.1:p.=
ENST00000496967.1:n.213+2142T>A