Linked Data
gnomAD v4:
4-67754376-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67754376C>T , CM000666.2:g.67754376C>T | GRCh38 |
| NC_000004.11:g.68620094C>T , CM000666.1:g.68620094C>T | GRCh37 |
| NC_000004.10:g.68302689C>T | NCBI36 |
| NG_009293.1:g.6711G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226413.5:c.-41G>A MANE Select | ENSP00000226413.5:n.-41G>A | |
| NM_000406.2:c.-41G>A | NP_000397.1:n.-41G>A | |
| NM_001012763.1:c.-41G>A | NP_001012781.1:n.-41G>A | |
| NM_000406.3:c.-41G>A MANE Select | NP_000397.1:n.-41G>A | |
| NM_001012763.2:c.-41G>A | NP_001012781.1:n.-41G>A |