Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21739650T>A , CM000669.2:g.21739650T>A | GRCh38 |
| NC_000007.13:g.21779268T>A , CM000669.1:g.21779268T>A | GRCh37 |
| NC_000007.12:g.21745793T>A | NCBI36 |
| NG_012886.2:g.201436T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001277115.2:c.7891T>A MANE Select | NP_001264044.1:p.Phe2631Ile |
| ENST00000409508.8:c.7891T>A MANE Select | ENSP00000475939.1:p.Phe2631Ile |
| NM_001277115.1:c.7891T>A | NP_001264044.1:p.Phe2631Ile |
| ENST00000328843.10:c.7912T>A | ENSP00000330671.7:p.Phe2638Ile |
| ENST00000409508.7:c.7891T>A | ENSP00000475939.1:p.Phe2631Ile |
| ENST00000605912.1:c.451T>A | ENSP00000476068.1:p.Phe151Ile |
| ENST00000620169.4:c.7912T>A | ENSP00000481693.1:p.Phe2638Ile |