Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128261761C>A , CM000667.2:g.128261761C>A | GRCh38 |
| NC_000005.9:g.127597453C>A , CM000667.1:g.127597453C>A | GRCh37 |
| NC_000005.8:g.127625352C>A | NCBI36 |
| NG_008750.1:g.281283G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262464.9:c.8339G>T MANE Select | ENSP00000262464.4:p.Ser2780Ile | |
| ENST00000262464.8:c.8339G>T | ENSP00000262464.4:p.Ser2780Ile | |
| ENST00000508053.5:c.8339G>T | ENSP00000424571.1:p.Ser2780Ile | |
| ENST00000619499.4:c.8336G>T | ENSP00000482132.1:p.Ser2779Ile | |
| NM_001999.3:c.8339G>T | NP_001990.2:p.Ser2780Ile | |
| XM_017009228.2:c.8186G>T | XP_016864717.1:p.Ser2729Ile | |
| NM_001999.4:c.8339G>T MANE Select | NP_001990.2:p.Ser2780Ile |