Linked Data
gnomAD v4:
1-1014014-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1014014G>A , CM000663.2:g.1014014G>A | GRCh38 |
| NC_000001.10:g.949394G>A , CM000663.1:g.949394G>A | GRCh37 |
| NC_000001.9:g.939257G>A | NCBI36 |
| NG_033033.1:g.5548G>A | |
| NG_033033.2:g.17877G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000624697.4:c.10G>A | ENSP00000485643.1:p.Gly4Ser | |
| ENST00000649529.1:c.34G>A MANE Select | ENSP00000496832.1:p.Gly12Ser | |
| ENST00000379389.4:c.34G>A | ENSP00000368699.4:p.Gly12Ser | |
| ENST00000624652.1:c.10G>A | ENSP00000485313.1:p.Gly4Ser | |
| ENST00000624697.3:c.10G>A | ENSP00000485643.1:p.Gly4Ser | |
| NM_005101.3:c.34G>A | NP_005092.1:p.Gly12Ser | |
| NM_005101.4:c.34G>A MANE Select | NP_005092.1:p.Gly12Ser |