Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48364929T>A , CM000675.2:g.48364929T>A | GRCh38 |
| NC_000013.10:g.48939065T>A , CM000675.1:g.48939065T>A | GRCh37 |
| NC_000013.9:g.47837066T>A | NCBI36 |
| NG_009009.1:g.66183T>A , LRG_517:g.66183T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000321.3:c.897T>A MANE Select | NP_000312.2:p.Phe299Leu |
| ENST00000267163.6:c.897T>A MANE Select | ENSP00000267163.4:p.Phe299Leu |
| NM_000321.2:c.897T>A , LRG_517t1:c.897T>A | NP_000312.2:p.Phe299Leu |
| ENST00000267163.4:c.897T>A | ENSP00000267163.4:p.Phe299Leu |
| ENST00000650461.1:c.897T>A | ENSP00000497193.1:p.Phe299Leu |
| XM_011535171.1:c.636T>A | XP_011533473.1:p.Phe212Leu |
| XM_011535171.2:c.636T>A | XP_011533473.1:p.Phe212Leu |
| XR_002957522.1:n.169A>T |