Linked Data
gnomAD v4:
12-4911989-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4911989G>T , CM000674.2:g.4911989G>T | GRCh38 |
| NC_000012.11:g.5021155G>T , CM000674.1:g.5021155G>T | GRCh37 |
| NC_000012.10:g.4891416G>T | NCBI36 |
| NG_011815.1:g.7083G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.611G>T MANE Select | ENSP00000371985.3:p.Arg204Leu | |
| ENST00000543874.3:n.105+1517G>T | ||
| ENST00000639306.1:c.449G>T | ENSP00000492506.1:p.Arg150Leu | |
| ENST00000382545.3:c.611G>T | ENSP00000371985.3:p.Arg204Leu | |
| ENST00000541095.1:n.105+1517G>T | ||
| ENST00000543874.2:n.96+1517G>T | ||
| NM_000217.2:c.611G>T | NP_000208.2:p.Arg204Leu | |
| NM_000217.3:c.611G>T MANE Select | NP_000208.2:p.Arg204Leu |