Linked Data
gnomAD v4:
17-43755326-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43755326G>T , CM000679.2:g.43755326G>T | GRCh38 |
| NC_000017.10:g.41832694G>T , CM000679.1:g.41832694G>T | GRCh37 |
| NC_000017.9:g.39188220G>T | NCBI36 |
| NG_008078.2:g.8463C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301691.3:c.*16C>A MANE Select | ENSP00000301691.1:n.*16C>A | |
| ENST00000301691.2:c.*16C>A | ENSP00000301691.1:n.*16C>A | |
| NM_025237.2:c.*16C>A | NP_079513.1:n.*16C>A | |
| NM_025237.3:c.*16C>A MANE Select | NP_079513.1:n.*16C>A |