Linked Data
gnomAD v4:
11-121307366-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.121307366G>T , CM000673.2:g.121307366G>T | GRCh38 |
| NC_000011.9:g.121178075G>T , CM000673.1:g.121178075G>T | GRCh37 |
| NC_000011.8:g.120683285G>T | NCBI36 |
| NG_009446.1:g.19688G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264027.9:c.754G>T MANE Select | ENSP00000264027.4:p.Gly252Cys | |
| ENST00000264027.8:c.754G>T | ENSP00000264027.4:p.Gly252Cys | |
| ENST00000392789.2:c.754G>T | ENSP00000376539.2:p.Gly252Cys | |
| ENST00000527183.1:n.1047G>T | ||
| ENST00000534230.5:c.632-91G>T | ENSP00000432550.1:n.632-91G>T | |
| NM_001024956.2:c.754G>T | NP_001020127.1:p.Gly252Cys | |
| NM_006918.4:c.754G>T | NP_008849.2:p.Gly252Cys | |
| NM_006918.5:c.754G>T MANE Select | NP_008849.2:p.Gly252Cys | |
| NM_001024956.3:c.754G>T | NP_001020127.1:p.Gly252Cys |