Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.29773607T= , CM000675.2:g.29773607T= | GRCh38 |
| NC_000013.10:g.30347744T= , CM000675.1:g.30347744T= | GRCh37 |
| NC_000013.9:g.29245744T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_007106.4:c.137-1409A= MANE Select | NP_009037.1:n.137-1409A= |
| ENST00000380680.5:c.137-1409A= MANE Select | ENSP00000370055.4:n.137-1409A= |
| NM_007106.3:c.137-1409A= | NP_009037.1:n.137-1409A= |
| ENST00000380680.4:c.137-1409A= | ENSP00000370055.4:n.137-1409A= |
| XM_011535123.1:c.113-1409A= | XP_011533425.1:n.113-1409A= |