Linked Data
gnomAD v4:
11-108147604-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108147604G>T , CM000673.2:g.108147604G>T | GRCh38 |
| NC_000011.9:g.108018331G>T , CM000673.1:g.108018331G>T | GRCh37 |
| NC_000011.8:g.107523541G>T | NCBI36 |
| NG_009888.1:g.31074G>T | |
| NG_009888.2:g.35900G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265838.8:c.*214G>T | ENSP00000265838.4:n.*214G>T | |
| NM_000019.3:c.*214G>T | NP_000010.1:n.*214G>T | |
| XM_006718834.2:c.*214G>T | XP_006718897.1:n.*214G>T | |
| XM_006718835.2:c.*214G>T | XP_006718898.1:n.*214G>T | |
| XM_017017682.2:c.*214G>T | XP_016873171.1:n.*214G>T | |
| XM_017017683.2:c.*214G>T | XP_016873172.1:n.*214G>T |