Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.114044068T>A , CM000672.2:g.114044068T>A | GRCh38 |
| NC_000010.10:g.115803827T>A , CM000672.1:g.115803827T>A | GRCh37 |
| NC_000010.9:g.115793817T>A | NCBI36 |
| NG_012187.1:g.5022T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369295.4:c.-65T>A MANE Select | ENSP00000358301.2:n.-65T>A | |
| ENST00000369295.3:c.-65T>A | ENSP00000358301.2:n.-65T>A | |
| NM_000684.2:c.-65T>A | NP_000675.1:n.-65T>A | |
| NM_000684.3:c.-65T>A MANE Select | NP_000675.1:n.-65T>A |