Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22365894T= , CM000673.2:g.22365894T= | GRCh38 |
| NC_000011.9:g.22387440T= , CM000673.1:g.22387440T= | GRCh37 |
| NC_000011.8:g.22344016T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020346.3:c.891+205T= MANE Select | NP_065079.1:n.891+205T= |
| ENST00000263160.4:c.891+205T= MANE Select | ENSP00000263160.3:n.891+205T= |
| NM_020346.2:c.891+205T= | NP_065079.1:n.891+205T= |
| ENST00000263160.3:c.891+205T= | ENSP00000263160.3:n.891+205T= |
| ENST00000648880.1:n.574T= |