Linked Data
gnomAD v4:
22-36564818-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.36564818A>C , CM000684.2:g.36564818A>C | GRCh38 |
| NC_000022.10:g.36960865A>C , CM000684.1:g.36960865A>C | GRCh37 |
| NC_000022.9:g.35290811A>C | NCBI36 |
| NG_031861.1:g.142826T>G | |
| NG_031861.2:g.143041T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300105.7:c.505T>G MANE Select | ENSP00000300105.6:p.Ser169Ala | |
| ENST00000300105.6:c.505T>G | ENSP00000300105.6:p.Ser169Ala | |
| NM_006078.3:c.505T>G | NP_006069.1:p.Ser169Ala | |
| NM_006078.4:c.505T>G | NP_006069.1:p.Ser169Ala | |
| XM_017028531.2:c.247T>G | XP_016884020.1:p.Ser83Ala | |
| NM_001379051.1:c.436T>G | NP_001365980.1:p.Ser146Ala | |
| NM_006078.5:c.505T>G MANE Select | NP_006069.1:p.Ser169Ala | |
| NR_166440.1:n.1871T>G |