Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48364929T= , CM000675.2:g.48364929T= | GRCh38 |
| NC_000013.10:g.48939065T= , CM000675.1:g.48939065T= | GRCh37 |
| NC_000013.9:g.47837066T= | NCBI36 |
| NG_009009.1:g.66183T= , LRG_517:g.66183T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.897T= MANE Select | ENSP00000267163.4:p.Phe299= | |
| ENST00000650461.1:c.897T= | ENSP00000497193.1:p.Phe299= | |
| ENST00000267163.4:c.897T= | ENSP00000267163.4:p.Phe299= | |
| NM_000321.2:c.897T= , LRG_517t1:c.897T= | NP_000312.2:p.Phe299= | |
| XM_011535171.1:c.636T= | XP_011533473.1:p.Phe212= | |
| XM_011535171.2:c.636T= | XP_011533473.1:p.Phe212= | |
| XR_002957522.1:n.169A= | ||
| NM_000321.3:c.897T= MANE Select | NP_000312.2:p.Phe299= |