Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149927647C= , CM000663.2:g.149927647C= | GRCh38 |
| NC_000001.10:g.149899539C= , CM000663.1:g.149899539C= | GRCh37 |
| NC_000001.9:g.148166163C= | NCBI36 |
| NG_032777.1:g.5606G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.9:c.34+79G= MANE Select | ENSP00000271628.8:n.34+79G= | |
| ENST00000271628.8:c.34+79G= | ENSP00000271628.8:n.34+79G= | |
| NM_005850.4:c.34+79G= | NP_005841.1:n.34+79G= | |
| NM_005850.5:c.34+79G= MANE Select | NP_005841.1:n.34+79G= |