MyVariant.info:
GRCh38
chr19:g.41237956G>C
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41237956G>C , CM000681.2:g.41237956G>C | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301178.9:c.796G>C MANE Select | ENSP00000301178.3:p.Asp266His | |
| ENST00000301178.8:c.796G>C | ENSP00000301178.3:p.Asp266His | |
| ENST00000359092.7:c.796G>C | ENSP00000351995.2:p.Asp266His | |
| ENST00000593513.1:c.-9G>C | ENSP00000471497.1:n.-9G>C | |
| ENST00000599659.5:n.810G>C | ||
| NM_001278599.1:c.-9G>C | NP_001265528.1:n.-9G>C | |
| NM_001699.5:c.796G>C | NP_001690.2:p.Asp266His | |
| NM_021913.4:c.796G>C | NP_068713.2:p.Asp266His | |
| NM_021913.5:c.796G>C MANE Select | NP_068713.2:p.Asp266His | |
| NM_001699.6:c.796G>C | NP_001690.2:p.Asp266His | |
| NM_001278599.2:c.-9G>C | NP_001265528.1:n.-9G>C |