Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.55231650C>A , CM000667.2:g.55231650C>A | GRCh38 |
| NC_000005.9:g.54527478C>A , CM000667.1:g.54527478C>A | GRCh37 |
| NC_000005.8:g.54563235C>A | NCBI36 |
| NG_034201.1:g.7068G>T | |
| NG_051620.1:g.666G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282572.5:c.778G>T MANE Select | ENSP00000282572.4:p.Ala260Ser | |
| ENST00000282572.4:c.778G>T | ENSP00000282572.4:p.Ala260Ser | |
| ENST00000501463.2:c.*758G>T | ENSP00000422485.1:n.*758G>T | |
| NM_021147.4:c.778G>T | NP_066970.3:p.Ala260Ser | |
| NR_125346.1:n.1348G>T | ||
| NR_125347.1:n.977G>T | ||
| NR_125348.1:n.842G>T | ||
| NM_021147.5:c.778G>T MANE Select | NP_066970.3:p.Ala260Ser | |
| NR_125346.2:n.1239G>T | ||
| NR_125347.2:n.868G>T |