Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.70452021C>G , CM000685.2:g.70452021C>G | GRCh38 |
| NC_000023.10:g.69671871C>G , CM000685.1:g.69671871C>G | GRCh37 |
| NC_000023.9:g.69588596C>G | NCBI36 |
| NG_015849.1:g.12167C>G | |
| NG_015849.2:g.12167C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374360.8:c.1140C>G MANE Select | ENSP00000363480.3:p.Phe380Leu | |
| ENST00000194900.8:c.1194C>G | ENSP00000194900.4:p.Phe398Leu | |
| ENST00000374360.7:c.1140C>G | ENSP00000363480.3:p.Phe380Leu | |
| ENST00000463252.5:n.1539C>G | ||
| NM_021120.3:c.1140C>G | NP_066943.2:p.Phe380Leu | |
| XM_006724625.2:c.1140C>G | XP_006724688.1:p.Phe380Leu | |
| XM_006724626.2:c.1140C>G | XP_006724689.1:p.Phe380Leu | |
| XM_011530883.1:c.1140C>G | XP_011529185.1:p.Phe380Leu | |
| NM_021120.4:c.1140C>G MANE Select | NP_066943.2:p.Phe380Leu |