dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.76731998A>T , CM000667.2:g.76731998A>T | GRCh38 |
| NC_000005.9:g.76027823A>T , CM000667.1:g.76027823A>T | GRCh37 |
| NC_000005.8:g.76063579A>T | NCBI36 |
| NG_032906.1:g.20956A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319211.5:c.89-316A>T MANE Select | ENSP00000321326.4:n.89-316A>T | |
| ENST00000319211.4:c.89-316A>T | ENSP00000321326.4:n.89-316A>T | |
| NM_001311313.1:c.-275-316A>T | NP_001298242.1:n.-275-316A>T | |
| NM_001992.3:c.89-316A>T | NP_001983.2:n.89-316A>T | |
| NM_001992.4:c.89-316A>T | NP_001983.2:n.89-316A>T | |
| NM_001992.5:c.89-316A>T MANE Select | NP_001983.2:n.89-316A>T | |
| NM_001311313.2:c.-275-316A>T | NP_001298242.1:n.-275-316A>T |