Linked Data
gnomAD v4:
X-78117901-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.78117901C>A , CM000685.2:g.78117901C>A | GRCh38 |
| NC_000023.10:g.77373398C>A , CM000685.1:g.77373398C>A | GRCh37 |
| NC_000023.9:g.77260054C>A | NCBI36 |
| NG_008862.1:g.18733C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373316.5:c.522-150C>A MANE Select | ENSP00000362413.4:n.522-150C>A | |
| ENST00000644362.1:c.438-150C>A | ENSP00000496140.1:n.438-150C>A | |
| ENST00000373316.4:c.522-150C>A | ENSP00000362413.4:n.522-150C>A | |
| ENST00000491291.1:n.514-150C>A | ||
| NM_000291.3:c.522-150C>A | NP_000282.1:n.522-150C>A | |
| NM_000291.4:c.522-150C>A MANE Select | NP_000282.1:n.522-150C>A |