Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71124372G= , CM000664.2:g.71124372G= | GRCh38 |
| NC_000002.11:g.71351502G= , CM000664.1:g.71351502G= | GRCh37 |
| NC_000002.10:g.71205010G= | NCBI36 |
| NG_008977.1:g.10893C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000244217.6:c.212C= MANE Select | ENSP00000244217.5:p.Ala71= | |
| ENST00000244217.5:c.212C= | ENSP00000244217.5:p.Ala71= | |
| ENST00000413592.5:c.80C= | ENSP00000391140.1:p.Ala27= | |
| ENST00000486135.1:c.-74C= | ENSP00000441569.1:n.-74C= | |
| ENST00000494660.6:c.-74C= | ENSP00000437361.1:n.-74C= | |
| NM_032601.3:c.212C= | NP_115990.3:p.Ala71= | |
| XM_005264613.2:c.212C= | XP_005264670.1:p.Ala71= | |
| XR_939729.1:n.281C= | ||
| XR_939729.2:n.281C= | ||
| NM_032601.4:c.212C= MANE Select | NP_115990.3:p.Ala71= |