Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1985908C>A , CM000678.2:g.1985908C>A | GRCh38 |
| NC_000016.9:g.2035909C>A , CM000678.1:g.2035909C>A | GRCh37 |
| NC_000016.8:g.1975910C>A | NCBI36 |
| NG_016288.1:g.6760C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.273C>A | ENSP00000455885.1:p.Phe91Leu | |
| ENST00000248114.7:c.498C>A MANE Select | ENSP00000248114.6:p.Phe166Leu | |
| ENST00000248114.6:c.498C>A | ENSP00000248114.6:p.Phe166Leu | |
| ENST00000565658.1:n.655C>A | ||
| ENST00000567719.1:c.273C>A | ENSP00000455885.1:p.Phe91Leu | |
| ENST00000569451.1:c.301C>A | ENSP00000456432.1:p.His101Asn | |
| NM_005262.2:c.498C>A | NP_005253.3:p.Phe166Leu | |
| NM_005262.3:c.498C>A MANE Select | NP_005253.3:p.Phe166Leu |