Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102842732A>G , CM000673.2:g.102842732A>G | GRCh38 |
| NC_000011.9:g.102713463A>G , CM000673.1:g.102713463A>G | GRCh37 |
| NC_000011.8:g.102218673A>G | NCBI36 |
| NG_012100.1:g.5880T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299855.10:c.290T>C MANE Select | ENSP00000299855.5:p.Val97Ala | |
| ENST00000299855.9:c.290T>C | ENSP00000299855.5:p.Val97Ala | |
| ENST00000524478.1:c.*132T>C | ENSP00000435255.1:n.*132T>C | |
| NM_002422.3:c.290T>C | NP_002413.1:p.Val97Ala | |
| NM_002422.4:c.290T>C | NP_002413.1:p.Val97Ala | |
| NM_002422.5:c.290T>C MANE Select | NP_002413.1:p.Val97Ala |