Linked Data
gnomAD v4:
4-67740432-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67740432A>T , CM000666.2:g.67740432A>T | GRCh38 |
| NC_000004.11:g.68606150A>T , CM000666.1:g.68606150A>T | GRCh37 |
| NC_000004.10:g.68288745A>T | NCBI36 |
| NG_009293.1:g.20655T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226413.5:c.*48T>A MANE Select | ENSP00000226413.5:n.*48T>A | |
| ENST00000226413.4:c.*48T>A | ENSP00000226413.4:n.*48T>A | |
| NM_000406.2:c.*48T>A | NP_000397.1:n.*48T>A | |
| NM_001012763.1:c.*157T>A | NP_001012781.1:n.*157T>A | |
| NM_000406.3:c.*48T>A MANE Select | NP_000397.1:n.*48T>A | |
| NM_001012763.2:c.*157T>A | NP_001012781.1:n.*157T>A |