Linked Data
gnomAD v4:
4-68670630-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68670630G>T , CM000666.2:g.68670630G>T | GRCh38 |
| NC_000004.11:g.69536348G>T , CM000666.1:g.69536348G>T | GRCh37 |
| NC_000004.10:g.69218943G>T | NCBI36 |
| NG_052676.1:g.5147C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338206.6:c.-12C>A MANE Select | ENSP00000341045.5:n.-12C>A | |
| NM_001076.3:c.-12C>A | NP_001067.2:n.-12C>A | |
| NM_001076.4:c.-12C>A MANE Select | NP_001067.2:n.-12C>A |