Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.23048049C>A , CM000682.2:g.23048049C>A | GRCh38 |
| NC_000020.10:g.23028686C>A , CM000682.1:g.23028686C>A | GRCh37 |
| NC_000020.9:g.22976686C>A | NCBI36 |
| NG_012027.1:g.6616G>T , LRG_168:g.6616G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000361.3:c.1456G>T MANE Select | NP_000352.1:p.Asp486Tyr |
| ENST00000377103.3:c.1456G>T MANE Select | ENSP00000366307.2:p.Asp486Tyr |
| NM_000361.2:c.1456G>T , LRG_168t1:c.1456G>T | NP_000352.1:p.Asp486Tyr |
| ENST00000377103.2:c.1456G>T | ENSP00000366307.2:p.Asp486Tyr |