Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.69648079C>A , CM000673.2:g.69648079C>A | GRCh38 |
| NC_000011.9:g.69462847C>A , CM000673.1:g.69462847C>A | GRCh37 |
| NC_000011.8:g.69172028C>A | NCBI36 |
| NG_007375.1:g.11975C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227507.3:c.660C>A MANE Select | ENSP00000227507.2:p.Pro220= | |
| ENST00000227507.2:c.660C>A | ENSP00000227507.2:p.Pro220= | |
| ENST00000536559.1:c.*80C>A | ENSP00000438482.1:n.*80C>A | |
| ENST00000542367.1:n.123C>A | ||
| ENST00000545484.1:n.366C>A | ||
| NM_053056.2:c.660C>A | NP_444284.1:p.Pro220= | |
| XM_006718653.2:c.684C>A | XP_006718716.1:p.Pro228= | |
| NM_053056.3:c.660C>A MANE Select | NP_444284.1:p.Pro220= |