LDH info
Identifiers and link-outs to other resources
ClinVar Variation Id:
1801
User contributed link-outs
Genomic Alleles
HGVS |
Genome Assembly |
NC_000010.11:g.102837281G>T , CM000672.2:g.102837281G>T
|
GRCh38
|
NC_000010.10:g.104597038G>T , CM000672.1:g.104597038G>T
|
GRCh37
|
NC_000010.9:g.104587028G>T
|
NCBI36
|
NG_007955.1:g.5253C>A
|
|
Transcript Alleles
HGVS |
Amino-acid change |
NM_000102.3:c.81C>A
VV
|
NP_000093.1:p.Tyr27Ter
|
|
NM_000102.4:c.81C>A
VV
MANE Preferred
|
NP_000093.1:p.Tyr27Ter
|
|
ENST00000369887.3:c.81C>A
|
ENSP00000358903.3:p.Tyr27Ter
|
|
ENST00000489268.1:n.134C>A
|
|
|