Linked Data
gnomAD v4:
9-134408158-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134408158C>A , CM000671.2:g.134408158C>A | GRCh38 |
| NC_000009.11:g.137300004C>A , CM000671.1:g.137300004C>A | GRCh37 |
| NC_000009.10:g.136439825C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000481739.2:c.289C>A MANE Select | ENSP00000419692.1:p.Pro97Thr | |
| ENST00000672570.1:c.208C>A | ENSP00000500402.1:p.Pro70Thr | |
| ENST00000356384.4:n.699C>A | ||
| ENST00000481739.1:c.289C>A | ENSP00000419692.1:p.Pro97Thr | |
| NM_001291920.1:c.208C>A | NP_001278849.1:p.Pro70Thr | |
| NM_001291921.1:c.-3C>A | NP_001278850.1:n.-3C>A | |
| NM_002957.5:c.289C>A | NP_002948.1:p.Pro97Thr | |
| NM_002957.6:c.289C>A MANE Select | NP_002948.1:p.Pro97Thr | |
| NM_001291921.2:c.-3C>A | NP_001278850.1:n.-3C>A | |
| NM_001291920.2:c.208C>A | NP_001278849.1:p.Pro70Thr |