Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.30313565C= , CM000672.2:g.30313565C= | GRCh38 |
| NC_000010.10:g.30602494C= , CM000672.1:g.30602494C= | GRCh37 |
| NC_000010.9:g.30642500C= | NCBI36 |
| NG_028096.1:g.40774G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263063.9:c.*44G= MANE Select | ENSP00000263063.3:n.*44G= | |
| ENST00000263063.8:c.*44G= | ENSP00000263063.3:n.*44G= | |
| ENST00000488290.5:n.3548G= | ||
| NM_018109.3:c.*44G= | NP_060579.3:n.*44G= | |
| NM_018109.4:c.*44G= MANE Select | NP_060579.3:n.*44G= |