Linked Data
dbSNP Id:
rs781858497
ExAC:
X:50658822 A / G
gnomAD v2:
X-50658822-A-G
gnomAD v4:
X-50915822-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50915822A>G , CM000685.2:g.50915822A>G | GRCh38 |
| NC_000023.10:g.50658822A>G , CM000685.1:g.50658822A>G | GRCh37 |
| NC_000023.9:g.50675562A>G | NCBI36 |
| NG_012894.1:g.10039A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252677.4:c.394A>G MANE Select | ENSP00000252677.3:p.Arg132Gly | |
| ENST00000252677.3:c.394A>G | ENSP00000252677.3:p.Arg132Gly | |
| NM_005448.2:c.394A>G MANE Select | NP_005439.2:p.Arg132Gly |