Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94781859G= , CM000672.2:g.94781859G= | GRCh38 |
| NC_000010.10:g.96541616G= , CM000672.1:g.96541616G= | GRCh37 |
| NC_000010.9:g.96531606G= | NCBI36 |
| NG_008384.2:g.24154G= | |
| NG_008384.3:g.24179G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371321.9:c.681G= MANE Select | ENSP00000360372.3:p.Pro227= | |
| ENST00000645461.1:n.1734G= | ||
| ENST00000371321.7:c.681G= | ENSP00000360372.3:p.Pro227= | |
| ENST00000464755.1:c.1444G= | ENSP00000483243.1:n.1444G= | |
| NM_000769.2:c.681G= | NP_000760.1:p.Pro227= | |
| NM_000769.4:c.681G= MANE Select | NP_000760.1:p.Pro227= |