Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134835097G>A , CM000671.2:g.134835097G>A | GRCh38 |
| NC_000009.11:g.137726943G>A , CM000671.1:g.137726943G>A | GRCh37 |
| NC_000009.10:g.136866764G>A | NCBI36 |
| NG_008030.1:g.198292G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371820.4:c.5263G>A | ENSP00000360885.4:p.Ala1755Thr | |
| ENST00000371817.8:c.5263G>A MANE Select | ENSP00000360882.3:p.Ala1755Thr | |
| ENST00000371817.7:c.5263G>A | ENSP00000360882.3:p.Ala1755Thr | |
| ENST00000371820.3:c.521G>A | ||
| ENST00000618395.4:c.5263G>A | ENSP00000481360.1:p.Ala1755Thr | |
| NM_000093.4:c.5263G>A | NP_000084.3:p.Ala1755Thr | |
| NM_001278074.1:c.5263G>A | NP_001265003.1:p.Ala1755Thr | |
| NR_103451.2:n.71-14888C>T | ||
| NM_000093.5:c.5263G>A MANE Select | NP_000084.3:p.Ala1755Thr |