LDH info

Canonical Allele Identifier: CA8051301
Gene: NOD2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2067085

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50699948C>A , CM000678.2:g.50699948C>A GRCh38
NC_000016.9:g.50733859C>A , CM000678.1:g.50733859C>A GRCh37
NC_000016.8:g.49291360C>A NCBI36
NG_007508.1:g.7810C>A , LRG_177:g.7810C>A

Transcript Alleles

HGVS Amino-acid change
NM_001293557.1:c.453C>A VV NP_001280486.1:p.Ser151=
NM_022162.2:c.534C>A VV NP_071445.1:p.Ser178=
XM_005256084.2:c.453C>A XP_005256141.1:p.Ser151=
XM_006721242.2:c.453C>A XP_006721305.1:p.Ser151=
XM_006721243.2:c.453C>A XP_006721306.1:p.Ser151=
XM_011523257.1:c.-44C>A XP_011521559.1:p.=
XM_011523258.1:c.-38+6286C>A XP_011521560.1:p.=
XM_011523259.1:c.-27C>A XP_011521561.1:p.=
XM_011523260.1:c.453C>A XP_011521562.1:p.Ser151=
XM_011523261.1:c.453C>A XP_011521563.1:p.Ser151=
XR_429725.2:n.543C>A
XR_429726.2:n.543C>A
XR_933387.1:n.543C>A
XM_005256084.4:c.453C>A XP_005256141.1:p.Ser151=
XM_006721242.4:c.453C>A XP_006721305.1:p.Ser151=
XM_006721243.4:c.453C>A XP_006721306.1:p.Ser151=
XM_011523259.2:c.-27C>A XP_011521561.1:p.=
XM_011523260.3:c.453C>A XP_011521562.1:p.Ser151=
XM_011523261.2:c.453C>A XP_011521563.1:p.Ser151=
XM_017023536.1:c.-127+6286C>A XP_016879025.1:p.=
XM_017023537.1:c.-21+6286C>A XP_016879026.1:p.=
XR_429725.3:n.496C>A
XR_429726.3:n.496C>A
XR_933387.2:n.496C>A
NM_001293557.2:c.453C>A VV NP_001280486.1:p.Ser151=
NM_001370466.1:c.453C>A VV NP_001357395.1:p.Ser151=
NM_022162.3:c.534C>A VV NP_071445.1:p.Ser178=
NR_163434.1:n.518C>A
ENST00000300589.6:c.534C>A ENSP00000300589.2:p.Ser178=
ENST00000526417.6:n.521C>A
ENST00000527070.5:c.*1149C>A ENSP00000435149.1:p.=
ENST00000532206.1:n.638C>A