Linked Data
gnomAD v4:
4-41746090-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.41746090G>T , CM000666.2:g.41746090G>T | GRCh38 |
| NC_000004.11:g.41748107G>T , CM000666.1:g.41748107G>T | GRCh37 |
| NC_000004.10:g.41442864G>T | NCBI36 |
| NG_008243.1:g.7881C>A , LRG_513:g.7881C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226382.4:c.662C>A MANE Select | ENSP00000226382.2:p.Ala221Asp | |
| ENST00000226382.3:c.662C>A | ENSP00000226382.2:p.Ala221Asp | |
| ENST00000510424.2:n.483C>A | ||
| NM_003924.3:c.662C>A , LRG_513t1:c.662C>A | NP_003915.2:p.Ala221Asp | |
| NM_003924.4:c.662C>A MANE Select | NP_003915.2:p.Ala221Asp |