Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50139999A>G , CM000676.2:g.50139999A>G | GRCh38 |
| NC_000014.8:g.50606717A>G , CM000676.1:g.50606717A>G | GRCh37 |
| NC_000014.7:g.49676467A>G | NCBI36 |
| NG_051073.1:g.96695T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006939.4:c.2728T>C MANE Select | NP_008870.2:p.Phe910Leu |
| ENST00000216373.10:c.2728T>C MANE Select | ENSP00000216373.5:p.Phe910Leu |
| NM_006939.2:c.2728T>C | NP_008870.2:p.Phe910Leu |
| NM_006939.3:c.2728T>C | NP_008870.2:p.Phe910Leu |
| ENST00000216373.9:c.2728T>C | ENSP00000216373.5:p.Phe910Leu |
| ENST00000543680.5:c.2629T>C | ENSP00000445328.1:p.Phe877Leu |
| XM_005268021.1:c.2548T>C | XP_005268078.1:p.Phe850Leu |
| XM_011537103.1:c.2689T>C | XP_011535405.1:p.Phe897Leu |
| XM_011537104.1:c.2728T>C | XP_011535406.1:p.Phe910Leu |