Linked Data
dbSNP Id:
rs782122211
gnomAD v2:
X-77373333-A-G
gnomAD v3:
X-78117836-A-G
gnomAD v4:
X-78117836-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.78117836A>G , CM000685.2:g.78117836A>G | GRCh38 |
| NC_000023.10:g.77373333A>G , CM000685.1:g.77373333A>G | GRCh37 |
| NC_000023.9:g.77259989A>G | NCBI36 |
| NG_008862.1:g.18668A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373316.5:c.522-215A>G MANE Select | ENSP00000362413.4:n.522-215A>G | |
| ENST00000644362.1:c.438-215A>G | ENSP00000496140.1:n.438-215A>G | |
| ENST00000373316.4:c.522-215A>G | ENSP00000362413.4:n.522-215A>G | |
| ENST00000491291.1:n.514-215A>G | ||
| NM_000291.3:c.522-215A>G | NP_000282.1:n.522-215A>G | |
| NM_000291.4:c.522-215A>G MANE Select | NP_000282.1:n.522-215A>G |