Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.55232982G= , CM000667.2:g.55232982G= | GRCh38 |
| NC_000005.9:g.54528810G= , CM000667.1:g.54528810G= | GRCh37 |
| NC_000005.8:g.54564567G= | NCBI36 |
| NG_034201.1:g.5736C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282572.5:c.381+161C= MANE Select | ENSP00000282572.4:n.381+161C= | |
| ENST00000282572.4:c.381+161C= | ENSP00000282572.4:n.381+161C= | |
| ENST00000501463.2:c.*146C= | ENSP00000422485.1:n.*146C= | |
| NM_021147.4:c.381+161C= | NP_066970.3:n.381+161C= | |
| NR_125346.1:n.736C= | ||
| NR_125347.1:n.580+156C= | ||
| NR_125348.1:n.10C= | ||
| NM_021147.5:c.381+161C= MANE Select | NP_066970.3:n.381+161C= | |
| NR_125346.2:n.627C= | ||
| NR_125347.2:n.471+156C= |