Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.79919518T>A , CM000668.2:g.79919518T>A | GRCh38 |
| NC_000006.11:g.80629235T>A , CM000668.1:g.80629235T>A | GRCh37 |
| NC_000006.10:g.80685954T>A | NCBI36 |
| NG_009108.1:g.33081A>T | |
| NG_009108.2:g.33081A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_022726.4:c.571A>T MANE Select | NP_073563.1:p.Ile191Phe |
| ENST00000369816.5:c.571A>T MANE Select | ENSP00000358831.4:p.Ile191Phe |
| NM_022726.3:c.571A>T | NP_073563.1:p.Ile191Phe |
| ENST00000369816.4:c.571A>T | ENSP00000358831.4:p.Ile191Phe |