Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48410933T>G , CM000677.2:g.48410933T>G | GRCh38 |
| NC_000015.9:g.48703130T>G , CM000677.1:g.48703130T>G | GRCh37 |
| NC_000015.8:g.46490422T>G | NCBI36 |
| NG_008805.2:g.239856A>C , LRG_778:g.239856A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.*1481A>C | ENSP00000453958.2:n.*1481A>C | |
| ENST00000682158.1:n.2054A>C | ||
| ENST00000682170.1:n.2854A>C | ||
| ENST00000682767.1:n.1970A>C | ||
| ENST00000316623.10:c.*57A>C MANE Select | ENSP00000325527.5:n.*57A>C | |
| ENST00000316623.9:c.*57A>C | ENSP00000325527.5:n.*57A>C | |
| ENST00000559133.5:c.4042A>C | ||
| NM_000138.4:c.*57A>C , LRG_778t1:c.*57A>C | NP_000129.3:n.*57A>C | |
| NM_000138.5:c.*57A>C MANE Select | NP_000129.3:n.*57A>C |