LDH info

Canonical Allele Identifier: CA15072662
Gene: PER3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs228642

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7803233C>T , CM000663.2:g.7803233C>T GRCh38
NC_000001.10:g.7863293C>T , CM000663.1:g.7863293C>T GRCh37
NC_000001.9:g.7785880C>T NCBI36
NG_046850.1:g.23854C>T

Transcript Alleles

HGVS Amino-acid change
NM_001289861.1:c.979+80C>T VV NP_001276790.1:p.=
NM_001289862.1:c.979+80C>T VV NP_001276791.1:p.=
NM_001289863.1:c.979+80C>T VV NP_001276792.1:p.=
NM_001289864.1:c.22+80C>T VV NP_001276793.1:p.=
NM_016831.2:c.976+80C>T VV NP_058515.1:p.=
XM_005263521.2:c.979+80C>T XP_005263578.1:p.=
XM_005263522.2:c.976+80C>T XP_005263579.1:p.=
XM_005263523.2:c.979+80C>T XP_005263580.1:p.=
XM_005263524.2:c.979+80C>T XP_005263581.1:p.=
XM_005263529.2:c.454+80C>T XP_005263586.1:p.=
XM_011542384.1:c.979+80C>T XP_011540686.1:p.=
XM_011542385.1:c.979+80C>T XP_011540687.1:p.=
XM_011542386.1:c.979+80C>T XP_011540688.1:p.=
XM_011542387.1:c.811+80C>T XP_011540689.1:p.=
XM_011542388.1:c.631+80C>T XP_011540690.1:p.=
XM_011542389.1:c.616+80C>T XP_011540691.1:p.=
XM_011542390.1:c.979+80C>T XP_011540692.1:p.=
XM_005263524.4:c.979+80C>T XP_005263581.1:p.=
XM_017002723.2:c.976+80C>T XP_016858212.1:p.=
XM_017002724.2:c.976+80C>T XP_016858213.1:p.=
XM_017002726.2:c.976+80C>T XP_016858215.1:p.=
XM_017002727.1:c.811+80C>T XP_016858216.1:p.=
XM_017002728.1:c.631+80C>T XP_016858217.1:p.=
XM_017002729.1:c.616+80C>T XP_016858218.1:p.=
XM_017002730.2:c.631+80C>T XP_016858219.1:p.=
XM_017002731.2:c.631+80C>T XP_016858220.1:p.=
XM_017002732.1:c.631+80C>T XP_016858221.1:p.=
XM_017002733.2:c.454+80C>T XP_016858222.1:p.=
XM_017002734.1:c.454+80C>T XP_016858223.1:p.=
XM_017002735.2:c.454+80C>T XP_016858224.1:p.=
XM_017002737.1:c.-287+80C>T XP_016858226.1:p.=
XM_017002738.2:c.-287+80C>T XP_016858227.1:p.=
XM_024450585.1:c.979+80C>T XP_024306353.1:p.=
XM_024450586.1:c.979+80C>T XP_024306354.1:p.=
XM_024450587.1:c.979+80C>T XP_024306355.1:p.=
XM_024450588.1:c.979+80C>T XP_024306356.1:p.=
XM_024450590.1:c.976+80C>T XP_024306358.1:p.=
XM_024450611.1:c.454+80C>T XP_024306379.1:p.=
XM_024450612.1:c.454+80C>T XP_024306380.1:p.=
NM_001289861.2:c.979+80C>T VV NP_001276790.1:p.=
NM_001289862.2:c.979+80C>T VV NP_001276791.1:p.=
NM_001289863.3:c.979+80C>T VV NP_001276792.1:p.=
NM_001289864.3:c.22+80C>T VV NP_001276793.1:p.=
NM_001377275.1:c.979+80C>T VV NP_001364204.1:p.=
NM_001377276.1:c.979+80C>T VV NP_001364205.1:p.=
NM_016831.4:c.976+80C>T VV NP_058515.1:p.=
ENST00000361923.2:c.976+80C>T ENSP00000355031.2:p.=
ENST00000377532.7:c.979+80C>T ENSP00000366755.3:p.=
ENST00000377541.5:c.976+80C>T ENSP00000366764.1:p.=
ENST00000463106.1:n.103+80C>T
ENST00000613533.4:c.979+80C>T ENSP00000482093.1:p.=
ENST00000614998.4:c.979+80C>T ENSP00000479223.1:p.=