Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965804G>A , CM000670.2:g.37965804G>A | GRCh38 |
| NC_000008.10:g.37823322G>A , CM000670.1:g.37823322G>A | GRCh37 |
| NC_000008.9:g.37942479G>A | NCBI36 |
| NG_011936.1:g.5863C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000345060.5:c.666C>T MANE Select | ENSP00000343782.3:p.Phe222= | |
| ENST00000520341.2:n.794C>T | ||
| ENST00000647937.1:c.150C>T | ENSP00000497740.1:p.Phe50= | |
| ENST00000345060.4:c.666C>T | ENSP00000343782.3:p.Phe222= | |
| ENST00000614635.1:c.666C>T | ENSP00000480325.1:p.Phe222= | |
| NM_000025.2:c.666C>T | NP_000016.1:p.Phe222= | |
| NM_000025.3:c.666C>T MANE Select | NP_000016.1:p.Phe222= |