Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133373294G>T , CM000672.2:g.133373294G>T | GRCh38 |
| NC_000010.10:g.135186798G>T , CM000672.1:g.135186798G>T | GRCh37 |
| NC_000010.9:g.135036788G>T | NCBI36 |
| NG_042077.1:g.5111C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368547.4:c.40C>A MANE Select | ENSP00000357535.3:p.Pro14Thr | |
| ENST00000368547.3:c.40C>A | ENSP00000357535.3:p.Pro14Thr | |
| NM_004092.3:c.40C>A | NP_004083.3:p.Pro14Thr | |
| XR_002956965.1:n.103C>A | ||
| NM_004092.4:c.40C>A MANE Select | NP_004083.3:p.Pro14Thr |