Linked Data
ClinVar Variation Id:
215952
dbSNP Id:
rs146054214
ExAC:
16:3639865 G / A
gnomAD v2:
16-3639865-G-A
gnomAD v3:
16-3589864-G-A
gnomAD v4:
16-3589864-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3589864G>A , CM000678.2:g.3589864G>A | GRCh38 |
| NC_000016.9:g.3639865G>A , CM000678.1:g.3639865G>A | GRCh37 |
| NC_000016.8:g.3579866G>A | NCBI36 |
| NG_028123.1:g.26721C>T , LRG_503:g.26721C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000294008.4:c.3774C>T MANE Select | ENSP00000294008.3:p.Pro1258= | |
| ENST00000294008.3:c.3774C>T | ENSP00000294008.3:p.Pro1258= | |
| NM_032444.2:c.3774C>T , LRG_503t1:c.3774C>T | NP_115820.2:p.Pro1258= | |
| XM_011522715.1:c.3774C>T | XP_011521017.1:p.Pro1258= | |
| NM_032444.3:c.3774C>T | NP_115820.2:p.Pro1258= | |
| XM_011522715.3:c.3774C>T | XP_011521017.1:p.Pro1258= | |
| XM_017023775.2:c.2952C>T | XP_016879264.1:p.Pro984= | |
| XM_024450471.1:c.3774C>T | XP_024306239.1:p.Pro1258= | |
| NM_032444.4:c.3774C>T MANE Select | NP_115820.2:p.Pro1258= |