Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965503C>A , CM000670.2:g.37965503C>A | GRCh38 |
| NC_000008.10:g.37823021C>A , CM000670.1:g.37823021C>A | GRCh37 |
| NC_000008.9:g.37942178C>A | NCBI36 |
| NG_011936.1:g.6164G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000025.3:c.967G>T MANE Select | NP_000016.1:p.Val323Phe |
| ENST00000345060.5:c.967G>T MANE Select | ENSP00000343782.3:p.Val323Phe |
| NM_000025.2:c.967G>T | NP_000016.1:p.Val323Phe |
| ENST00000345060.4:c.967G>T | ENSP00000343782.3:p.Val323Phe |
| ENST00000520341.1:n.242G>T | |
| ENST00000520341.2:n.1095G>T | |
| ENST00000614635.1:c.967G>T | ENSP00000480325.1:p.Val323Phe |
| ENST00000647937.1:c.451G>T | ENSP00000497740.1:p.Val151Phe |