Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128357356G>A , CM000667.2:g.128357356G>A | GRCh38 |
| NC_000005.9:g.127693048G>A , CM000667.1:g.127693048G>A | GRCh37 |
| NC_000005.8:g.127720947G>A | NCBI36 |
| NG_008750.1:g.185688C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262464.9:c.2594C>T MANE Select | ENSP00000262464.4:p.Ala865Val | |
| ENST00000262464.8:c.2594C>T | ENSP00000262464.4:p.Ala865Val | |
| ENST00000508053.5:c.2594C>T | ENSP00000424571.1:p.Ala865Val | |
| ENST00000508989.5:c.2495C>T | ENSP00000425596.1:p.Ala832Val | |
| ENST00000619499.4:c.2591C>T | ENSP00000482132.1:p.Ala864Val | |
| NM_001999.3:c.2594C>T | NP_001990.2:p.Ala865Val | |
| XM_017009228.2:c.2441C>T | XP_016864717.1:p.Ala814Val | |
| NM_001999.4:c.2594C>T MANE Select | NP_001990.2:p.Ala865Val |