Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.81478714A>G , CM000670.2:g.81478714A>G | GRCh38 |
| NC_000008.10:g.82390949A>G , CM000670.1:g.82390949A>G | GRCh37 |
| NC_000008.9:g.82553504A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256104.5:c.*151T>C MANE Select | ENSP00000256104.4:n.*151T>C | |
| ENST00000256104.4:c.*151T>C | ENSP00000256104.4:n.*151T>C | |
| ENST00000518669.5:n.485T>C | ||
| ENST00000521734.1:n.759T>C | ||
| ENST00000522659.1:c.*426T>C | ENSP00000428385.1:n.*426T>C | |
| NM_001442.2:c.*151T>C | NP_001433.1:n.*151T>C | |
| XR_001745980.1:n.514+16740A>G | ||
| NM_001442.3:c.*151T>C MANE Select | NP_001433.1:n.*151T>C |