Linked Data
gnomAD v4:
8-19955952-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19955952C>T , CM000670.2:g.19955952C>T | GRCh38 |
| NC_000008.10:g.19813463C>T , CM000670.1:g.19813463C>T | GRCh37 |
| NC_000008.9:g.19857743C>T | NCBI36 |
| NG_008855.1:g.21882C>T | |
| NG_008855.2:g.59236C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.887C>T MANE Select | ENSP00000497642.1:p.Ala296Val | |
| ENST00000311322.8:c.887C>T | ENSP00000309757.6:p.Ala296Val | |
| NM_000237.2:c.887C>T | NP_000228.1:p.Ala296Val | |
| NM_000237.3:c.887C>T MANE Select | NP_000228.1:p.Ala296Val |