Linked Data
gnomAD v4:
1-40784077-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.40784077C>T , CM000663.2:g.40784077C>T | GRCh38 |
| NC_000001.10:g.41249749C>T , CM000663.1:g.41249749C>T | GRCh37 |
| NC_000001.9:g.41022336C>T | NCBI36 |
| NG_008139.1:g.5066C>T | |
| NG_008139.2:g.5066C>T | |
| NG_008139.3:g.5291C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000347132.10:c.-17C>T MANE Select | ENSP00000262916.6:n.-17C>T | |
| ENST00000347132.9:c.-17C>T | ENSP00000262916.6:n.-17C>T | |
| NM_004700.3:c.-17C>T | NP_004691.2:n.-17C>T | |
| NM_172163.2:c.-17C>T | NP_751895.1:n.-17C>T | |
| NM_004700.4:c.-17C>T MANE Select | NP_004691.2:n.-17C>T | |
| NM_172163.3:c.-17C>T | NP_751895.1:n.-17C>T |