Linked Data
gnomAD v4:
1-115033279-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115033279T>G , CM000663.2:g.115033279T>G | GRCh38 |
| NC_000001.10:g.115575900T>G , CM000663.1:g.115575900T>G | GRCh37 |
| NC_000001.9:g.115377423T>G | NCBI36 |
| NG_015891.1:g.8486T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256592.3:c.-1-83T>G MANE Select | ENSP00000256592.1:n.-1-83T>G | |
| ENST00000256592.2:c.-1-83T>G | ENSP00000256592.1:n.-1-83T>G | |
| NM_000549.4:c.-1-83T>G | NP_000540.2:n.-1-83T>G | |
| NM_000549.5:c.-1-83T>G MANE Select | NP_000540.2:n.-1-83T>G |