Linked Data
gnomAD v4:
17-43755771-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43755771G>A , CM000679.2:g.43755771G>A | GRCh38 |
| NC_000017.10:g.41833139G>A , CM000679.1:g.41833139G>A | GRCh37 |
| NC_000017.9:g.39188665G>A | NCBI36 |
| NG_008078.2:g.8018C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301691.3:c.221-8C>T MANE Select | ENSP00000301691.1:n.221-8C>T | |
| ENST00000301691.2:c.221-8C>T | ENSP00000301691.1:n.221-8C>T | |
| NM_025237.2:c.221-8C>T | NP_079513.1:n.221-8C>T | |
| NM_025237.3:c.221-8C>T MANE Select | NP_079513.1:n.221-8C>T |