Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.71994594G>A , CM000674.2:g.71994594G>A | GRCh38 |
| NC_000012.11:g.72388374G>A , CM000674.1:g.72388374G>A | GRCh37 |
| NC_000012.10:g.70674641G>A | NCBI36 |
| NG_008279.1:g.60749G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_173353.4:c.1068+29G>A MANE Select | NP_775489.2:n.1068+29G>A |
| ENST00000333850.4:c.1068+29G>A MANE Select | ENSP00000329093.3:n.1068+29G>A |
| NM_173353.3:c.1068+29G>A | NP_775489.2:n.1068+29G>A |
| ENST00000333850.3:c.1068+29G>A | ENSP00000329093.3:n.1068+29G>A |
| XM_011537899.1:c.474+29G>A | XP_011536201.1:n.474+29G>A |