Linked Data
gnomAD v4:
16-88719703-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88719703G>T , CM000678.2:g.88719703G>T | GRCh38 |
| NC_000016.9:g.88786111G>T , CM000678.1:g.88786111G>T | GRCh37 |
| NC_000016.8:g.87313612G>T | NCBI36 |
| NG_042229.1:g.70518C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301015.14:c.6342C>A MANE Select | ENSP00000301015.9:p.Phe2114Leu | |
| ENST00000466823.3:c.368C>A | ||
| ENST00000301015.13:c.6342C>A | ENSP00000301015.9:p.Phe2114Leu | |
| ENST00000419505.5:c.108C>A | ENSP00000406358.1:p.Phe36Leu | |
| ENST00000466823.2:c.368C>A | ||
| ENST00000495568.7:n.583C>A | ||
| ENST00000497793.2:n.497C>A | ||
| NM_001142864.2:c.6342C>A | NP_001136336.2:p.Phe2114Leu | |
| NM_001142864.3:c.6342C>A | NP_001136336.2:p.Phe2114Leu | |
| NM_001142864.4:c.6342C>A MANE Select | NP_001136336.2:p.Phe2114Leu |