Linked Data
gnomAD v4:
4-99420703-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99420703T>C , CM000666.2:g.99420703T>C | GRCh38 |
| NC_000004.11:g.100341860T>C , CM000666.1:g.100341860T>C | GRCh37 |
| NC_000004.10:g.100560883T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000437033.7:c.655A>G MANE Select | ENSP00000414254.2:p.Ile219Val | |
| ENST00000209665.8:c.691A>G | ENSP00000209665.4:p.Ile231Val | |
| ENST00000437033.6:c.655A>G | ENSP00000414254.2:p.Ile219Val | |
| ENST00000476959.5:c.715A>G | ENSP00000420269.1:p.Ile239Val | |
| ENST00000482593.5:c.484A>G | ENSP00000420613.1:p.Ile162Val | |
| NM_000673.4:c.691A>G | NP_000664.2:p.Ile231Val | |
| NM_001166504.1:c.715A>G | NP_001159976.1:p.Ile239Val | |
| NM_000673.7:c.655A>G MANE Select | NP_000664.3:p.Ile219Val | |
| NM_001166504.2:c.715A>G | NP_001159976.1:p.Ile239Val |