Linked Data
gnomAD v4:
4-55125559-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55125559A>T , CM000666.2:g.55125559A>T | GRCh38 |
| NC_000004.11:g.55991726A>T , CM000666.1:g.55991726A>T | GRCh37 |
| NC_000004.10:g.55686483A>T | NCBI36 |
| NG_012004.1:g.5037T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.-266T>A MANE Select | ENSP00000263923.4:n.-266T>A | |
| ENST00000263923.4:c.-266T>A | ENSP00000263923.4:n.-266T>A | |
| NM_002253.2:c.-266T>A | NP_002244.1:n.-266T>A | |
| NM_002253.3:c.-266T>A | NP_002244.1:n.-266T>A | |
| NM_002253.4:c.-266T>A MANE Select | NP_002244.1:n.-266T>A |