Linked Data
gnomAD v4:
1-58576709-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.58576709G>T , CM000663.2:g.58576709G>T | GRCh38 |
| NC_000001.10:g.59042381G>T , CM000663.1:g.59042381G>T | GRCh37 |
| NC_000001.9:g.58814969G>T | NCBI36 |
| NG_016237.1:g.5786C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371225.4:c.448C>A MANE Select | ENSP00000360269.2:p.Arg150Ser | |
| ENST00000371225.3:c.448C>A | ENSP00000360269.2:p.Arg150Ser | |
| NM_002353.2:c.448C>A | NP_002344.2:p.Arg150Ser | |
| NM_002353.3:c.448C>A MANE Select | NP_002344.2:p.Arg150Ser |