Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35500152C= , CM000668.2:g.35500152C= | GRCh38 |
| NC_000006.11:g.35467929C= , CM000668.1:g.35467929C= | GRCh37 |
| NC_000006.10:g.35575907C= | NCBI36 |
| NG_009077.1:g.17719G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229771.11:c.1324G= MANE Select | ENSP00000229771.6:p.Ala442= | |
| ENST00000229771.10:c.1324G= | ENSP00000229771.6:p.Ala442= | |
| ENST00000322263.8:c.1165G= | ENSP00000319414.4:p.Ala389= | |
| ENST00000495781.1:n.500G= | ||
| ENST00000614066.4:c.1318G= | ENSP00000477534.1:p.Ala440= | |
| NM_001289395.1:c.1165G= | NP_001276324.1:p.Ala389= | |
| NM_003322.4:c.1324G= | NP_003313.3:p.Ala442= | |
| NM_003322.5:c.1324G= | NP_003313.3:p.Ala442= | |
| NM_003322.6:c.1324G= MANE Select | NP_003313.3:p.Ala442= | |
| NM_001289395.2:c.1165G= | NP_001276324.1:p.Ala389= |