LDH info

Canonical Allele Identifier: CA211435
Gene: GCH1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 161248
dbSNP Id: rs200891969

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.54845784C>T , CM000676.2:g.54845784C>T GRCh38
NC_000014.8:g.55312502C>T , CM000676.1:g.55312502C>T GRCh37
NC_000014.7:g.54382252C>T NCBI36
NG_008647.1:g.62041G>A

Transcript Alleles

HGVS Amino-acid change
NM_000161.2:c.610G>A VV NP_000152.1:p.Val204Ile
NM_001024024.1:c.610G>A VV NP_001019195.1:p.Val204Ile
NM_001024070.1:c.610G>A VV NP_001019241.1:p.Val204Ile
NM_001024071.1:c.610G>A VV NP_001019242.1:p.Val204Ile
XM_005267530.1:c.610G>A XP_005267587.1:p.Val204Ile
XM_017021218.1:c.316G>A XP_016876707.1:p.Val106Ile
NM_000161.3:c.610G>A VV MANE Preferred NP_000152.1:p.Val204Ile
ENST00000254299.8:n.758G>A
ENST00000395514.5:c.610G>A ENSP00000378890.1:p.Val204Ile
ENST00000395521.6:n.293-2730G>A
ENST00000491895.6:c.610G>A ENSP00000419045.2:p.Val204Ile
ENST00000536224.2:c.610G>A ENSP00000445246.2:p.Val204Ile
ENST00000543643.6:c.610G>A ENSP00000444011.2:p.Val204Ile
ENST00000622544.4:c.610G>A ENSP00000477796.1:p.Val204Ile