Linked Data
gnomAD v4:
19-18388978-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18388978A>G , CM000681.2:g.18388978A>G | GRCh38 |
| NC_000019.9:g.18499788A>G , CM000681.1:g.18499788A>G | GRCh37 |
| NC_000019.8:g.18360788A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252809.3:c.*43A>G MANE Select | ENSP00000252809.3:n.*43A>G | |
| NM_004864.2:c.*43A>G | NP_004855.2:n.*43A>G | |
| NM_004864.3:c.*43A>G | NP_004855.2:n.*43A>G | |
| XM_024451789.1:c.*43A>G | XP_024307557.1:n.*43A>G | |
| NM_004864.4:c.*43A>G MANE Select | NP_004855.2:n.*43A>G |