Linked Data
dbSNP Id:
rs782375610
ExAC:
X:153609078 C / G
gnomAD v2:
X-153609078-C-G
gnomAD v3:
X-154380718-C-G
gnomAD v4:
X-154380718-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154380718C>G , CM000685.2:g.154380718C>G | GRCh38 |
| NC_000023.10:g.153609078C>G , CM000685.1:g.153609078C>G | GRCh37 |
| NC_000023.9:g.153262272C>G | NCBI36 |
| NG_008677.1:g.11283C>G , LRG_745:g.11283C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682114.1:c.400-35C>G | ENSP00000507245.1:n.400-35C>G | |
| ENST00000682478.1:n.590-35C>G | ||
| ENST00000683576.1:n.590-35C>G | ||
| ENST00000683627.1:c.400-35C>G | ENSP00000507533.1:n.400-35C>G | |
| ENST00000684082.1:c.357-35C>G | ENSP00000508266.1:n.357-35C>G | |
| ENST00000684633.1:n.372-35C>G | ||
| ENST00000684678.1:c.396-35C>G | ENSP00000507059.1:n.396-35C>G | |
| ENST00000369842.9:c.400-35C>G MANE Select | ENSP00000358857.4:n.400-35C>G | |
| ENST00000369835.3:c.295-35C>G | ENSP00000358850.3:n.295-35C>G | |
| ENST00000369842.8:c.400-35C>G | ENSP00000358857.4:n.400-35C>G | |
| ENST00000428228.5:c.*305-35C>G | ENSP00000401081.1:n.*305-35C>G | |
| ENST00000468294.5:n.360-35C>G | ||
| ENST00000471965.1:n.154C>G | ||
| ENST00000485261.1:n.590-35C>G | ||
| ENST00000486738.5:n.758-35C>G | ||
| ENST00000492448.1:n.383-35C>G | ||
| NM_000117.2:c.400-35C>G , LRG_745t1:c.400-35C>G | NP_000108.1:n.400-35C>G | |
| XM_024452349.1:c.406-35C>G | XP_024308117.1:n.406-35C>G | |
| NM_000117.3:c.400-35C>G MANE Select | NP_000108.1:n.400-35C>G |