Linked Data
ClinVar Variation Id:
2917092
ClinVar RCV Id:
RCV003615480
dbSNP Id:
rs1420313332
gnomAD v3:
15-73322928-T-C
gnomAD v4:
15-73322928-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73322928T>C , CM000677.2:g.73322928T>C | GRCh38 |
| NC_000015.9:g.73615269T>C , CM000677.1:g.73615269T>C | GRCh37 |
| NC_000015.8:g.71402322T>C | NCBI36 |
| NG_009063.1:g.51337A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.3165A>G MANE Select | ENSP00000261917.3:p.Pro1055= | |
| ENST00000261917.3:c.3165A>G | ENSP00000261917.3:p.Pro1055= | |
| NM_005477.2:c.3165A>G | NP_005468.1:p.Pro1055= | |
| XM_011521148.1:c.1947A>G | XP_011519450.1:p.Pro649= | |
| XM_011521148.2:c.1947A>G | XP_011519450.1:p.Pro649= | |
| NM_005477.3:c.3165A>G MANE Select | NP_005468.1:p.Pro1055= |