Linked Data
gnomAD v4:
1-155290153-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.155290153A>T , CM000663.2:g.155290153A>T | GRCh38 |
| NC_000001.10:g.155259944A>T , CM000663.1:g.155259944A>T | GRCh37 |
| NC_000001.9:g.153526568A>T | NCBI36 |
| NG_011677.1:g.16282T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342741.6:c.*419T>A MANE Select | ENSP00000339933.4:n.*419T>A | |
| ENST00000392414.7:c.*419T>A | ENSP00000376214.3:n.*419T>A | |
| NM_000298.5:c.*419T>A | NP_000289.1:n.*419T>A | |
| NM_181871.3:c.*419T>A | NP_870986.1:n.*419T>A | |
| NM_000298.6:c.*419T>A MANE Select | NP_000289.1:n.*419T>A | |
| NM_181871.4:c.*419T>A | NP_870986.1:n.*419T>A |