Linked Data
gnomAD v4:
14-23433761-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23433761C>T , CM000676.2:g.23433761C>T | GRCh38 |
| NC_000014.8:g.23902970C>T , CM000676.1:g.23902970C>T | GRCh37 |
| NC_000014.7:g.22972810C>T | NCBI36 |
| NG_007884.1:g.6901G>A , LRG_384:g.6901G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.-8-21G>A MANE Select | ENSP00000347507.3:n.-8-21G>A | |
| ENST00000355349.3:c.-8-21G>A | ENSP00000347507.3:n.-8-21G>A | |
| NM_000257.3:c.-8-21G>A | NP_000248.2:n.-8-21G>A | |
| XR_245686.3:n.99-21G>A | ||
| XM_017021340.1:c.-8-21G>A | XP_016876829.1:n.-8-21G>A | |
| NM_000257.4:c.-8-21G>A MANE Select | NP_000248.2:n.-8-21G>A |