Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31366070T>A , CM000664.2:g.31366070T>A | GRCh38 |
| NC_000002.11:g.31588936T>A , CM000664.1:g.31588936T>A | GRCh37 |
| NC_000002.10:g.31442440T>A | NCBI36 |
| NG_008871.1:g.53676A>T | |
| NG_008871.2:g.53676A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000379.4:c.2362A>T MANE Select | NP_000370.2:p.Ile788Phe |
| ENST00000379416.4:c.2362A>T MANE Select | ENSP00000368727.3:p.Ile788Phe |
| NM_000379.3:c.2362A>T | NP_000370.2:p.Ile788Phe |
| ENST00000379416.3:c.2362A>T | ENSP00000368727.3:p.Ile788Phe |
| XM_011533095.1:c.2359A>T | XP_011531397.1:p.Ile787Phe |
| XM_011533095.2:c.2359A>T | XP_011531397.1:p.Ile787Phe |
| XM_011533096.1:c.2362A>T | XP_011531398.1:p.Ile788Phe |
| XM_011533096.2:c.2362A>T | XP_011531398.1:p.Ile788Phe |