Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.179087953C>T , CM000663.2:g.179087953C>T | GRCh38 |
| NC_000001.10:g.179057088C>T , CM000663.1:g.179057088C>T | GRCh37 |
| NC_000001.9:g.177323711C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_022371.4:c.682C>T MANE Select | NP_071766.2:p.His228Tyr |
| ENST00000367627.8:c.682C>T MANE Select | ENSP00000356599.3:p.His228Tyr |
| NM_022371.3:c.682C>T | NP_071766.2:p.His228Tyr |
| ENST00000352445.10:c.682C>T | ENSP00000335351.6:p.His228Tyr |
| ENST00000367627.7:c.682C>T | ENSP00000356599.3:p.His228Tyr |
| ENST00000447595.1:c.358C>T | ENSP00000410195.1:p.His120Tyr |
| ENST00000472001.1:n.364C>T | |
| ENST00000483887.1:c.*609C>T | ENSP00000435744.1:n.*609C>T |
| ENST00000495145.1:n.139C>T |