Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57763748T>C , CM000674.2:g.57763748T>C | GRCh38 |
| NC_000012.11:g.58157531T>C , CM000674.1:g.58157531T>C | GRCh37 |
| NC_000012.10:g.56443798T>C | NCBI36 |
| NG_007076.1:g.8446A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000713544.1:c.1357A>G | ENSP00000518840.1:p.Asn453Asp | |
| ENST00000713545.1:c.*281A>G | ENSP00000518841.1:n.*281A>G | |
| ENST00000228606.9:c.1276A>G MANE Select | ENSP00000228606.4:p.Asn426Asp | |
| ENST00000228606.8:c.1276A>G | ENSP00000228606.4:p.Asn426Asp | |
| ENST00000547344.5:n.1415A>G | ||
| NM_000785.3:c.1276A>G | NP_000776.1:p.Asn426Asp | |
| NM_000785.4:c.1276A>G MANE Select | NP_000776.1:p.Asn426Asp |