Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.84425338A>G , CM000664.2:g.84425338A>G | GRCh38 |
| NC_000002.11:g.84652462A>G , CM000664.1:g.84652462A>G | GRCh37 |
| NC_000002.10:g.84505973A>G | NCBI36 |
| NG_016755.1:g.39125T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393868.7:c.1014+77T>C MANE Select | ENSP00000377446.2:n.1014+77T>C | |
| ENST00000651342.1:c.*454+77T>C | ENSP00000498471.1:n.*454+77T>C | |
| ENST00000393868.6:c.1014+77T>C | ENSP00000377446.2:n.1014+77T>C | |
| ENST00000484365.1:n.1522+77T>C | ||
| ENST00000491123.5:n.860+77T>C | ||
| NM_003849.3:c.1014+77T>C | NP_003840.2:n.1014+77T>C | |
| NM_003849.4:c.1014+77T>C MANE Select | NP_003840.2:n.1014+77T>C |