Linked Data
gnomAD v4:
9-33025477-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.33025477C>T , CM000671.2:g.33025477C>T | GRCh38 |
| NC_000009.11:g.33025475C>T , CM000671.1:g.33025475C>T | GRCh37 |
| NC_000009.10:g.33015475C>T | NCBI36 |
| NG_012821.2:g.4655G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330899.5:c.-11+94C>T MANE Select | ENSP00000369127.3:n.-11+94C>T | |
| ENST00000330899.4:c.-11+94C>T | ENSP00000369127.3:n.-11+94C>T | |
| ENST00000495015.5:n.98+94C>T | ||
| NM_001314039.1:c.-304+94C>T | NP_001300968.1:n.-304+94C>T | |
| NM_001539.2:c.-11+94C>T | NP_001530.1:n.-11+94C>T | |
| NM_001539.3:c.-11+94C>T | NP_001530.1:n.-11+94C>T | |
| NM_001539.4:c.-11+94C>T MANE Select | NP_001530.1:n.-11+94C>T | |
| NM_001314039.2:c.-304+94C>T | NP_001300968.1:n.-304+94C>T |