Linked Data
gnomAD v4:
2-84425369-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.84425369A>C , CM000664.2:g.84425369A>C | GRCh38 |
| NC_000002.11:g.84652493A>C , CM000664.1:g.84652493A>C | GRCh37 |
| NC_000002.10:g.84506004A>C | NCBI36 |
| NG_016755.1:g.39094T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393868.7:c.1014+46T>G MANE Select | ENSP00000377446.2:n.1014+46T>G | |
| ENST00000651342.1:c.*454+46T>G | ENSP00000498471.1:n.*454+46T>G | |
| ENST00000393868.6:c.1014+46T>G | ENSP00000377446.2:n.1014+46T>G | |
| ENST00000484365.1:n.1522+46T>G | ||
| ENST00000491123.5:n.860+46T>G | ||
| NM_003849.3:c.1014+46T>G | NP_003840.2:n.1014+46T>G | |
| NM_003849.4:c.1014+46T>G MANE Select | NP_003840.2:n.1014+46T>G |