Linked Data
gnomAD v4:
12-5044761-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5044761T>G , CM000674.2:g.5044761T>G | GRCh38 |
| NC_000012.11:g.5153927T>G , CM000674.1:g.5153927T>G | GRCh37 |
| NC_000012.10:g.5024188T>G | NCBI36 |
| NG_012198.1:g.5843T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.614T>G MANE Select | ENSP00000252321.3:p.Leu205Arg | |
| ENST00000252321.4:c.614T>G | ENSP00000252321.3:p.Leu205Arg | |
| NM_002234.3:c.614T>G | NP_002225.2:p.Leu205Arg | |
| NM_002234.4:c.614T>G MANE Select | NP_002225.2:p.Leu205Arg |