Linked Data
gnomAD v4:
5-174724596-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.174724596T>A , CM000667.2:g.174724596T>A | GRCh38 |
| NC_000005.9:g.174151599T>A , CM000667.1:g.174151599T>A | GRCh37 |
| NC_000005.8:g.174084205T>A | NCBI36 |
| NG_008124.1:g.5025T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239243.7:c.-64T>A MANE Select | ENSP00000239243.5:n.-64T>A | |
| ENST00000239243.6:c.-64T>A | ENSP00000239243.5:n.-64T>A | |
| NM_002449.4:c.-64T>A | NP_002440.2:n.-64T>A | |
| NM_001363626.1:c.-64T>A | NP_001350555.1:n.-64T>A | |
| NM_002449.5:c.-64T>A MANE Select | NP_002440.2:n.-64T>A | |
| NM_001363626.2:c.-64T>A | NP_001350555.1:n.-64T>A |