Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.55233607C= , CM000667.2:g.55233607C= | GRCh38 |
| NC_000005.9:g.54529435C= , CM000667.1:g.54529435C= | GRCh37 |
| NC_000005.8:g.54565192C= | NCBI36 |
| NG_034201.1:g.5111G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282572.5:c.-84G= MANE Select | ENSP00000282572.4:n.-84G= | |
| ENST00000282572.4:c.-84G= | ENSP00000282572.4:n.-84G= | |
| NM_021147.4:c.-84G= | NP_066970.3:n.-84G= | |
| NR_125346.1:n.111G= | ||
| NR_125347.1:n.111G= | ||
| NM_021147.5:c.-84G= MANE Select | NP_066970.3:n.-84G= | |
| NR_125346.2:n.2G= | ||
| NR_125347.2:n.2G= |