Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.47839335C= , CM000681.2:g.47839335C= | GRCh38 |
| NC_000019.9:g.48342592C= , CM000681.1:g.48342592C= | GRCh37 |
| NC_000019.8:g.53034404C= | NCBI36 |
| NG_008605.1:g.22494C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000554.6:c.268C= MANE Select | NP_000545.1:p.Arg90= |
| ENST00000221996.12:c.268C= MANE Select | ENSP00000221996.5:p.Arg90= |
| NM_000554.4:c.268C= | NP_000545.1:p.Arg90= |
| NM_000554.5:c.268C= | NP_000545.1:p.Arg90= |
| ENST00000221996.11:c.268C= | ENSP00000221996.5:p.Arg90= |
| ENST00000539067.5:c.268C= | ENSP00000445565.1:p.Arg90= |
| ENST00000613299.1:c.116C= | ENSP00000478106.1:p.Pro39= |