Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35500121T= , CM000668.2:g.35500121T= | GRCh38 |
| NC_000006.11:g.35467898T= , CM000668.1:g.35467898T= | GRCh37 |
| NC_000006.10:g.35575876T= | NCBI36 |
| NG_009077.1:g.17750A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229771.11:c.1355A= MANE Select | ENSP00000229771.6:p.Asn452= | |
| ENST00000229771.10:c.1355A= | ENSP00000229771.6:p.Asn452= | |
| ENST00000322263.8:c.1196A= | ENSP00000319414.4:p.Asn399= | |
| ENST00000495781.1:n.531A= | ||
| ENST00000614066.4:c.1349A= | ENSP00000477534.1:p.Asn450= | |
| NM_001289395.1:c.1196A= | NP_001276324.1:p.Asn399= | |
| NM_003322.4:c.1355A= | NP_003313.3:p.Asn452= | |
| NM_003322.5:c.1355A= | NP_003313.3:p.Asn452= | |
| NM_003322.6:c.1355A= MANE Select | NP_003313.3:p.Asn452= | |
| NM_001289395.2:c.1196A= | NP_001276324.1:p.Asn399= |