Linked Data
gnomAD v4:
X-43949837-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.43949837A>G , CM000685.2:g.43949837A>G | GRCh38 |
| NC_000023.10:g.43809083A>G , CM000685.1:g.43809083A>G | GRCh37 |
| NC_000023.9:g.43694027A>G | NCBI36 |
| NG_009832.1:g.28839T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000642620.1:c.364T>C (NDP) MANE Select | ENSP00000495972.1:p.Tyr122His | |
| ENST00000647044.1:c.364T>C (NDP) | ENSP00000495811.1:p.Tyr122His | |
| ENST00000378062.5:c.364T>C (NDP) | ENSP00000367301.5:p.Tyr122His | |
| ENST00000470584.1:n.408T>C (NDP) | ||
| NM_000266.3:c.364T>C (NDP) | NP_000257.1:p.Tyr122His | |
| NR_046631.1:n.106A>G (NDP-AS1) | ||
| NM_000266.4:c.364T>C (NDP) MANE Select | NP_000257.1:p.Tyr122His |