Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.64615534T>A , CM000670.2:g.64615534T>A | GRCh38 |
| NC_000008.10:g.65528091T>A , CM000670.1:g.65528091T>A | GRCh37 |
| NC_000008.9:g.65690645T>A | NCBI36 |
| NG_008338.1:g.188258A>T | |
| NG_008338.2:g.188258A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310193.4:c.850+157A>T MANE Select | ENSP00000310721.3:n.850+157A>T | |
| ENST00000310193.3:c.850+157A>T | ENSP00000310721.3:n.850+157A>T | |
| ENST00000523954.1:n.124+157A>T | ||
| NM_004820.3:c.850+157A>T | NP_004811.1:n.850+157A>T | |
| NM_001324112.1:c.850+157A>T | NP_001311041.1:n.850+157A>T | |
| NM_004820.4:c.850+157A>T | NP_004811.1:n.850+157A>T | |
| XM_017014002.1:c.916+157A>T | XP_016869491.1:n.916+157A>T | |
| NM_004820.5:c.850+157A>T MANE Select | NP_004811.1:n.850+157A>T | |
| NM_001324112.2:c.850+157A>T | NP_001311041.1:n.850+157A>T |