Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134843197T>A , CM000671.2:g.134843197T>A | GRCh38 |
| NC_000009.11:g.137735043T>A , CM000671.1:g.137735043T>A | GRCh37 |
| NC_000009.10:g.136874864T>A | NCBI36 |
| NG_008030.1:g.206392T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371820.4:c.*894T>A | ENSP00000360885.4:n.*894T>A | |
| ENST00000371817.8:c.*894T>A MANE Select | ENSP00000360882.3:n.*894T>A | |
| ENST00000371817.7:c.*894T>A | ENSP00000360882.3:n.*894T>A | |
| ENST00000618395.4:c.*894T>A | ENSP00000481360.1:n.*894T>A | |
| NM_000093.4:c.*894T>A | NP_000084.3:n.*894T>A | |
| NM_001278074.1:c.*894T>A | NP_001265003.1:n.*894T>A | |
| NR_103451.2:n.71-22988A>T | ||
| NM_000093.5:c.*894T>A MANE Select | NP_000084.3:n.*894T>A |