Linked Data
ClinVar Variation Id:
2176995
ClinVar RCV Id:
RCV002585312
dbSNP Id:
rs1434063620
gnomAD v2:
16-89986088-A-T
gnomAD v4:
16-89919680-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89919680A>T , CM000678.2:g.89919680A>T | GRCh38 |
| NC_000016.9:g.89986088A>T , CM000678.1:g.89986088A>T | GRCh37 |
| NC_000016.8:g.88513589A>T | NCBI36 |
| NG_012026.1:g.6802A>T | |
| NG_027810.1:g.2672A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000555147.2:c.422A>T MANE Select | ENSP00000451605.1:p.Asp141Val | |
| ENST00000639847.1:c.422A>T | ENSP00000492011.1:p.Asp141Val | |
| ENST00000555147.1:c.422A>T | ENSP00000451605.1:p.Asp141Val | |
| ENST00000555427.1:c.422A>T | ENSP00000451760.1:p.Asp141Val | |
| ENST00000556922.1:c.422A>T | ENSP00000451560.1:p.Asp141Val | |
| NM_002386.3:c.422A>T | NP_002377.4:p.Asp141Val | |
| NM_002386.4:c.422A>T MANE Select | NP_002377.4:p.Asp141Val |