LDH info

Canonical Allele Identifier: CA99611099
Gene: PRKG2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10033237

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.81201633A>G , CM000666.2:g.81201633A>G GRCh38
NC_000004.11:g.82122787A>G , CM000666.1:g.82122787A>G GRCh37
NC_000004.10:g.82341811A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001282485.1:c.461+2954T>C VV NP_001269414.1:p.=
NM_006259.2:c.461+2954T>C VV NP_006250.1:p.=
XM_005263126.2:c.461+2954T>C XP_005263183.1:p.=
XM_011532114.1:c.461+2954T>C XP_011530416.1:p.=
XM_011532115.1:c.461+2954T>C XP_011530417.1:p.=
XM_011532116.1:c.461+2954T>C XP_011530418.1:p.=
NM_001363401.1:c.461+2954T>C VV NP_001350330.1:p.=
XM_017008413.1:c.461+2954T>C XP_016863902.1:p.=
XM_017008414.1:c.461+2954T>C XP_016863903.1:p.=
XM_017008415.1:c.461+2954T>C XP_016863904.1:p.=
XM_017008416.1:c.461+2954T>C XP_016863905.1:p.=
XM_017008417.1:c.461+2954T>C XP_016863906.1:p.=
XM_017008418.1:c.461+2954T>C XP_016863907.1:p.=
ENST00000264399.5:c.461+2954T>C ENSP00000264399.1:p.=
ENST00000395578.3:c.461+2954T>C ENSP00000378945.1:p.=
ENST00000628926.1:c.461+2954T>C ENSP00000486129.1:p.=