Linked Data
gnomAD v4:
1-1013949-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.1013949G>T , CM000663.2:g.1013949G>T | GRCh38 |
| NC_000001.10:g.949329G>T , CM000663.1:g.949329G>T | GRCh37 |
| NC_000001.9:g.939192G>T | NCBI36 |
| NG_033033.1:g.5483G>T | |
| NG_033033.2:g.17812G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000624697.4:c.-21-35G>T | ENSP00000485643.1:n.-21-35G>T | |
| ENST00000649529.1:c.4-35G>T MANE Select | ENSP00000496832.1:n.4-35G>T | |
| ENST00000379389.4:c.4-35G>T | ENSP00000368699.4:n.4-35G>T | |
| ENST00000624652.1:c.-21-35G>T | ENSP00000485313.1:n.-21-35G>T | |
| ENST00000624697.3:c.-21-35G>T | ENSP00000485643.1:n.-21-35G>T | |
| NM_005101.3:c.4-35G>T | NP_005092.1:n.4-35G>T | |
| NM_005101.4:c.4-35G>T MANE Select | NP_005092.1:n.4-35G>T |