Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52676315T>A , CM000674.2:g.52676315T>A | GRCh38 |
| NC_000012.11:g.53070099T>A , CM000674.1:g.53070099T>A | GRCh37 |
| NC_000012.10:g.51356366T>A | NCBI36 |
| NG_008364.1:g.9093A>T | |
| NG_008364.2:g.9093A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006121.4:c.1435A>T MANE Select | NP_006112.3:p.Ile479Phe |
| ENST00000252244.3:c.1435A>T MANE Select | ENSP00000252244.3:p.Ile479Phe |
| NM_006121.3:c.1435A>T | NP_006112.3:p.Ile479Phe |
| ENST00000548765.1:n.509A>T |