Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.55233503G>T , CM000667.2:g.55233503G>T | GRCh38 |
| NC_000005.9:g.54529331G>T , CM000667.1:g.54529331G>T | GRCh37 |
| NC_000005.8:g.54565088G>T | NCBI36 |
| NG_034201.1:g.5215C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282572.5:c.21C>A MANE Select | ENSP00000282572.4:p.Thr7= | |
| ENST00000282572.4:c.21C>A | ENSP00000282572.4:p.Thr7= | |
| ENST00000501463.2:c.21C>A | ENSP00000422485.1:p.Thr7= | |
| NM_021147.4:c.21C>A | NP_066970.3:p.Thr7= | |
| NR_125346.1:n.215C>A | ||
| NR_125347.1:n.215C>A | ||
| NM_021147.5:c.21C>A MANE Select | NP_066970.3:p.Thr7= | |
| NR_125346.2:n.106C>A | ||
| NR_125347.2:n.106C>A |