Linked Data
gnomAD v4:
1-115033321-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115033321G>A , CM000663.2:g.115033321G>A | GRCh38 |
| NC_000001.10:g.115575942G>A , CM000663.1:g.115575942G>A | GRCh37 |
| NC_000001.9:g.115377465G>A | NCBI36 |
| NG_015891.1:g.8528G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256592.3:c.-1-41G>A MANE Select | ENSP00000256592.1:n.-1-41G>A | |
| ENST00000256592.2:c.-1-41G>A | ENSP00000256592.1:n.-1-41G>A | |
| NM_000549.4:c.-1-41G>A | NP_000540.2:n.-1-41G>A | |
| XM_011542065.1:c.-42G>A | XP_011540367.1:n.-42G>A | |
| XM_011542065.2:c.-42G>A | XP_011540367.1:n.-42G>A | |
| NM_000549.5:c.-1-41G>A MANE Select | NP_000540.2:n.-1-41G>A |