Linked Data
gnomAD v4:
17-14208639-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.14208639G>T , CM000679.2:g.14208639G>T | GRCh38 |
| NC_000017.10:g.14111956G>T , CM000679.1:g.14111956G>T | GRCh37 |
| NC_000017.9:g.14052681G>T | NCBI36 |
| NG_008034.1:g.144238G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261643.8:c.*1426G>T MANE Select | ENSP00000261643.3:n.*1426G>T | |
| ENST00000664217.1:c.*141G>T | ENSP00000499396.1:n.*141G>T | |
| ENST00000670279.1:c.929-870G>T | ENSP00000499450.1:n.929-870G>T | |
| ENST00000261643.7:c.*1426G>T | ENSP00000261643.3:n.*1426G>T | |
| NM_001303.3:c.*1426G>T | NP_001294.2:n.*1426G>T | |
| XM_011523658.1:c.*1426G>T | XP_011521960.1:n.*1426G>T | |
| XR_933974.1:n.1032-870G>T | ||
| NM_001303.4:c.*1426G>T MANE Select | NP_001294.2:n.*1426G>T |