Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67942559G>A , CM000678.2:g.67942559G>A | GRCh38 |
| NC_000016.9:g.67976462G>A , CM000678.1:g.67976462G>A | GRCh37 |
| NC_000016.8:g.66533963G>A | NCBI36 |
| NG_009778.1:g.6554C>T | |
| NG_033098.1:g.31136C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000229.2:c.552C>T MANE Select | NP_000220.1:p.Leu184= |
| ENST00000264005.10:c.552C>T MANE Select | ENSP00000264005.5:p.Leu184= |
| NM_000229.1:c.552C>T | NP_000220.1:p.Leu184= |
| ENST00000264005.9:c.552C>T | ENSP00000264005.5:p.Leu184= |
| ENST00000570369.5:c.155+302C>T | |
| ENST00000570980.1:c.336C>T | ENSP00000464651.1:p.Leu112= |
| ENST00000573538.5:c.195C>T | ENSP00000463220.1:p.Leu65= |
| ENST00000573846.1:n.166C>T | |
| ENST00000575277.1:n.413C>T | |
| ENST00000575467.5:c.*247C>T | ENSP00000460653.1:n.*247C>T |
| ENST00000576450.1:c.19C>T |