Linked Data
dbSNP Id:
rs781950237
ExAC:
X:152959549 C / T
gnomAD v2:
X-152959549-C-T
gnomAD v3:
X-153694094-C-T
gnomAD v4:
X-153694094-C-T
COSMIC:
COSN23017595
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153694094C>T , CM000685.2:g.153694094C>T | GRCh38 |
| NC_000023.10:g.152959549C>T , CM000685.1:g.152959549C>T | GRCh37 |
| NC_000023.9:g.152612743C>T | NCBI36 |
| NG_012016.1:g.10798C>T | |
| NG_012016.2:g.10798C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253122.10:c.1255-36C>T MANE Select | ENSP00000253122.5:n.1255-36C>T | |
| ENST00000253122.9:c.1255-36C>T | ENSP00000253122.5:n.1255-36C>T | |
| ENST00000413787.1:c.258-110C>T | ENSP00000400463.1:n.258-110C>T | |
| ENST00000430077.6:c.910-36C>T | ENSP00000403041.2:n.910-36C>T | |
| ENST00000442457.1:c.309-36C>T | ||
| ENST00000457723.1:c.239-43C>T | ENSP00000394742.1:n.239-43C>T | |
| ENST00000485324.1:n.1364C>T | ||
| NM_001142805.1:c.1225-36C>T | NP_001136277.1:n.1225-36C>T | |
| NM_001142806.1:c.910-36C>T | NP_001136278.1:n.910-36C>T | |
| NM_005629.3:c.1255-36C>T | NP_005620.1:n.1255-36C>T | |
| NM_005629.4:c.1255-36C>T MANE Select | NP_005620.1:n.1255-36C>T | |
| NM_001142805.2:c.1225-36C>T | NP_001136277.1:n.1225-36C>T |