Linked Data
gnomAD v4:
4-55346241-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55346241T>A , CM000666.2:g.55346241T>A | GRCh38 |
| NC_000004.11:g.56212408T>A , CM000666.1:g.56212408T>A | GRCh37 |
| NC_000004.10:g.55907165T>A | NCBI36 |
| NG_028230.1:g.5021T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000679707.1:c.-96T>A | ENSP00000505713.1:n.-96T>A | |
| ENST00000679836.1:c.-96T>A | ENSP00000506601.1:n.-96T>A | |
| ENST00000264228.8:c.-96T>A | ENSP00000264228.4:n.-96T>A | |
| NM_024592.4:c.-96T>A | NP_078868.1:n.-96T>A | |
| XM_005265767.3:c.-96T>A | XP_005265824.1:n.-96T>A |