Linked Data
ClinVar Variation Id:
1417232
ClinVar RCV Id:
RCV001948092
dbSNP Id:
rs1016027191
gnomAD v3:
15-73367723-G-C
gnomAD v4:
15-73367723-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73367723G>C , CM000677.2:g.73367723G>C | GRCh38 |
| NC_000015.9:g.73660064G>C , CM000677.1:g.73660064G>C | GRCh37 |
| NC_000015.8:g.71447117G>C | NCBI36 |
| NG_009063.1:g.6542C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.548C>G MANE Select | ENSP00000261917.3:p.Ser183Trp | |
| ENST00000261917.3:c.548C>G | ENSP00000261917.3:p.Ser183Trp | |
| NM_005477.2:c.548C>G | NP_005468.1:p.Ser183Trp | |
| NM_005477.3:c.548C>G MANE Select | NP_005468.1:p.Ser183Trp |