Linked Data
dbSNP Id:
rs113574479
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.43949750A>T , CM000685.2:g.43949750A>T | GRCh38 |
| NC_000023.10:g.43808996A>T , CM000685.1:g.43808996A>T | GRCh37 |
| NC_000023.9:g.43693940A>T | NCBI36 |
| NG_009832.1:g.28926T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000642620.1:c.*49T>A (NDP) MANE Select | ENSP00000495972.1:n.*49T>A | |
| ENST00000647044.1:c.*49T>A (NDP) | ENSP00000495811.1:n.*49T>A | |
| ENST00000378062.5:c.*49T>A (NDP) | ENSP00000367301.5:n.*49T>A | |
| ENST00000470584.1:n.495T>A (NDP) | ||
| NM_000266.3:c.*49T>A (NDP) | NP_000257.1:n.*49T>A | |
| NR_046631.1:n.19A>T (NDP-AS1) | ||
| NM_000266.4:c.*49T>A (NDP) MANE Select | NP_000257.1:n.*49T>A |