Linked Data
ClinVar Variation Id:
1157535
ClinVar RCV Id:
RCV001500670
dbSNP Id:
rs782156020
ExAC:
X:148571869 T / C
gnomAD v2:
X-148571869-T-C
gnomAD v4:
X-149490338-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.149490338T>C , CM000685.2:g.149490338T>C | GRCh38 |
| NC_000023.10:g.148571869T>C , CM000685.1:g.148571869T>C | GRCh37 |
| NC_000023.9:g.148379774T>C | NCBI36 |
| NG_011900.3:g.19997A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340855.11:c.982A>G MANE Select | ENSP00000339801.6:p.Ile328Val | |
| ENST00000651111.1:c.349A>G | ENSP00000498395.1:p.Ile117Val | |
| ENST00000340855.10:c.982A>G | ENSP00000339801.6:p.Ile328Val | |
| ENST00000370441.8:c.982A>G | ENSP00000359470.4:p.Ile328Val | |
| ENST00000422081.6:c.349A>G | ENSP00000477056.1:p.Ile117Val | |
| ENST00000441880.1:n.114-3240A>G | ||
| ENST00000464251.5:c.908A>G | ENSP00000428980.1:n.908A>G | |
| ENST00000466323.5:c.*173A>G | ENSP00000418264.1:n.*173A>G | |
| ENST00000490775.5:n.767A>G | ||
| NM_000202.6:c.982A>G | NP_000193.1:p.Ile328Val | |
| NM_001166550.2:c.712A>G | NP_001160022.1:p.Ile238Val | |
| NM_006123.4:c.982A>G | NP_006114.1:p.Ile328Val | |
| NR_104128.1:n.1329A>G | ||
| NM_000202.7:c.982A>G | NP_000193.1:p.Ile328Val | |
| NM_001166550.3:c.712A>G | NP_001160022.1:p.Ile238Val | |
| NM_000202.8:c.982A>G MANE Select | NP_000193.1:p.Ile328Val | |
| NM_001166550.4:c.712A>G | NP_001160022.1:p.Ile238Val | |
| NM_006123.5:c.982A>G | NP_006114.1:p.Ile328Val | |
| NR_104128.2:n.1281A>G |