Linked Data
gnomAD v4:
X-50910755-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50910755G>T , CM000685.2:g.50910755G>T | GRCh38 |
| NC_000023.10:g.50653755G>T , CM000685.1:g.50653755G>T | GRCh37 |
| NC_000023.9:g.50670495G>T | NCBI36 |
| NG_012894.1:g.4972G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252677.4:c.-29G>T MANE Select | ENSP00000252677.3:n.-29G>T | |
| NM_005448.2:c.-29G>T MANE Select | NP_005439.2:n.-29G>T |