Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240874040A>T , CM000664.2:g.240874040A>T | GRCh38 |
| NC_000002.11:g.241813457A>T , CM000664.1:g.241813457A>T | GRCh37 |
| NC_000002.10:g.241462130A>T | NCBI36 |
| NG_008005.1:g.10296A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000030.3:c.658A>T MANE Select | NP_000021.1:p.Ile220Phe |
| ENST00000307503.4:c.658A>T MANE Select | ENSP00000302620.3:p.Ile220Phe |
| NM_000030.2:c.658A>T | NP_000021.1:p.Ile220Phe |
| ENST00000307503.3:c.658A>T | ENSP00000302620.3:p.Ile220Phe |
| ENST00000476698.1:n.332+991A>T |