LDH info

Canonical Allele Identifier: CA15041702
Gene: CSF2RA HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs28414810

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.1294564C>G , CM000685.2:g.1294564C>G GRCh38
NC_000023.10:g.1413457C>G , CM000685.1:g.1413457C>G GRCh37
NC_000023.9:g.1373457C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011546165.1:c.780+103C>G XP_011544467.1:p.=
XM_011546166.1:c.780+103C>G XP_011544468.1:p.=
XM_011546167.1:c.780+103C>G XP_011544469.1:p.=
XM_011546168.1:c.780+103C>G XP_011544470.1:p.=
XM_011546169.1:c.780+103C>G XP_011544471.1:p.=
XM_011546170.1:c.780+103C>G XP_011544472.1:p.=
XM_011546171.1:c.780+103C>G XP_011544473.1:p.=
XM_011546172.1:c.780+103C>G XP_011544474.1:p.=
XM_011546173.1:c.780+103C>G XP_011544475.1:p.=
XM_011546174.1:c.780+103C>G XP_011544476.1:p.=
XM_011546175.1:c.780+103C>G XP_011544477.1:p.=
XM_011546176.1:c.648+103C>G XP_011544478.1:p.=
XM_011546165.3:c.780+103C>G XP_011544467.1:p.=
XM_011546167.2:c.780+103C>G XP_011544469.1:p.=
XM_011546168.2:c.780+103C>G XP_011544470.1:p.=
XM_011546170.3:c.780+103C>G XP_011544472.1:p.=
XM_011546174.3:c.780+103C>G XP_011544476.1:p.=
XM_011546175.2:c.780+103C>G XP_011544477.1:p.=
XM_017029287.1:c.780+103C>G XP_016884776.1:p.=
XM_017029288.1:c.780+103C>G XP_016884777.1:p.=
ENST00000355432.8:c.780+103C>G ENSP00000347606.3:p.=
ENST00000355805.7:c.646+4055C>G ENSP00000348058.2:p.=
ENST00000381500.6:c.780+103C>G ENSP00000370911.1:p.=
ENST00000381509.8:c.780+103C>G ENSP00000370920.3:p.=
ENST00000381524.8:c.780+103C>G ENSP00000370935.3:p.=
ENST00000381529.8:c.780+103C>G ENSP00000370940.3:p.=
ENST00000417535.7:c.780+103C>G ENSP00000394227.2:p.=
ENST00000432318.7:c.780+103C>G ENSP00000416437.2:p.=
ENST00000475259.6:n.191+103C>G
ENST00000486791.6:c.780+103C>G ENSP00000436825.1:p.=
ENST00000491683.6:n.237+103C>G
ENST00000493312.6:n.817+103C>G
ENST00000494969.7:c.244+7366C>G ENSP00000476684.1:p.=
ENST00000498153.6:n.134+103C>G
ENST00000501036.7:c.381+103C>G ENSP00000440491.1:p.=