Linked Data
gnomAD v4:
12-14506929-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.14506929G>T , CM000674.2:g.14506929G>T | GRCh38 |
| NC_000012.11:g.14659863G>T , CM000674.1:g.14659863G>T | GRCh37 |
| NC_000012.10:g.14551130G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000240617.10:c.1372+4C>A MANE Select | ENSP00000240617.5:n.1372+4C>A | |
| ENST00000240617.9:c.1372+4C>A | ENSP00000240617.5:n.1372+4C>A | |
| NM_024829.5:c.1372+4C>A | NP_079105.4:n.1372+4C>A | |
| NM_024829.6:c.1372+4C>A MANE Select | NP_079105.4:n.1372+4C>A |