Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.182838256T= , CM000664.2:g.182838256T= | GRCh38 |
| NC_000002.11:g.183702984T= , CM000664.1:g.183702984T= | GRCh37 |
| NC_000002.10:g.183411229T= | NCBI36 |
| NG_017197.1:g.33515A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295113.5:c.797+153A= MANE Select | ENSP00000295113.4:n.797+153A= | |
| ENST00000295113.4:c.797+153A= | ENSP00000295113.4:n.797+153A= | |
| NM_001463.3:c.797+153A= | NP_001454.2:n.797+153A= | |
| NM_001463.4:c.797+153A= MANE Select | NP_001454.2:n.797+153A= |