Linked Data
ClinVar Variation Id:
542984
dbSNP Id:
rs140517685
ExAC:
21:47419073 G / A
gnomAD v2:
21-47419073-G-A
gnomAD v3:
21-45999159-G-A
gnomAD v4:
21-45999159-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45999159G>A , CM000683.2:g.45999159G>A | GRCh38 |
| NC_000021.8:g.47419073G>A , CM000683.1:g.47419073G>A | GRCh37 |
| NC_000021.7:g.46243501G>A | NCBI36 |
| NG_008674.1:g.22411G>A , LRG_475:g.22411G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361866.8:c.1681G>A MANE Select | ENSP00000355180.3:p.Asp561Asn | |
| ENST00000361866.7:c.1681G>A | ENSP00000355180.3:p.Asp561Asn | |
| ENST00000612273.1:c.1681G>A | ENSP00000483630.1:p.Asp561Asn | |
| NM_001848.2:c.1681G>A , LRG_475t1:c.1681G>A | NP_001839.2:p.Asp561Asn | |
| NM_001848.3:c.1681G>A MANE Select | NP_001839.2:p.Asp561Asn |