Linked Data
gnomAD v4:
2-218893213-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218893213G>T , CM000664.2:g.218893213G>T | GRCh38 |
| NC_000002.11:g.219757935G>T , CM000664.1:g.219757935G>T | GRCh37 |
| NC_000002.10:g.219466179G>T | NCBI36 |
| NG_012179.1:g.17681G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258411.8:c.1196G>T MANE Select | ENSP00000258411.3:p.Cys399Phe | |
| ENST00000258411.7:c.1196G>T | ENSP00000258411.3:p.Cys399Phe | |
| NM_025216.2:c.1196G>T | NP_079492.2:p.Cys399Phe | |
| XM_011511928.1:c.1145G>T | XP_011510230.1:p.Cys382Phe | |
| XM_011511929.1:c.1100G>T | XP_011510231.1:p.Cys367Phe | |
| XM_011511930.1:c.816G>T | XP_011510232.1:p.Val272= | |
| XM_011511929.2:c.1100G>T | XP_011510231.1:p.Cys367Phe | |
| NM_025216.3:c.1196G>T MANE Select | NP_079492.2:p.Cys399Phe |