Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128351001G>C , CM000667.2:g.128351001G>C | GRCh38 |
| NC_000005.9:g.127686693G>C , CM000667.1:g.127686693G>C | GRCh37 |
| NC_000005.8:g.127714592G>C | NCBI36 |
| NG_008750.1:g.192043C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262464.9:c.2679C>G MANE Select | ENSP00000262464.4:p.Ser893Arg | |
| ENST00000262464.8:c.2679C>G | ENSP00000262464.4:p.Ser893Arg | |
| ENST00000508053.5:c.2679C>G | ENSP00000424571.1:p.Ser893Arg | |
| ENST00000508989.5:c.2580C>G | ENSP00000425596.1:p.Ser860Arg | |
| ENST00000619499.4:c.2676C>G | ENSP00000482132.1:p.Ser892Arg | |
| NM_001999.3:c.2679C>G | NP_001990.2:p.Ser893Arg | |
| XM_017009228.2:c.2526C>G | XP_016864717.1:p.Ser842Arg | |
| NM_001999.4:c.2679C>G MANE Select | NP_001990.2:p.Ser893Arg |