Linked Data
gnomAD v4:
5-151259928-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.151259928G>T , CM000667.2:g.151259928G>T | GRCh38 |
| NC_000005.9:g.150639489G>T , CM000667.1:g.150639489G>T | GRCh37 |
| NC_000005.8:g.150619682G>T | NCBI36 |
| NG_009059.1:g.11877G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357164.4:c.243+12G>T MANE Select | ENSP00000349687.3:n.243+12G>T | |
| ENST00000357164.3:c.243+12G>T | ENSP00000349687.3:n.243+12G>T | |
| ENST00000523004.1:c.118+12G>T | ||
| ENST00000523466.5:c.288+12G>T | ENSP00000429100.1:n.288+12G>T | |
| NM_000405.4:c.243+12G>T | NP_000396.2:n.243+12G>T | |
| NM_001167607.1:c.243+12G>T | NP_001161079.1:n.243+12G>T | |
| NM_000405.5:c.243+12G>T MANE Select | NP_000396.2:n.243+12G>T | |
| NM_001167607.2:c.243+12G>T | NP_001161079.1:n.243+12G>T | |
| NM_001167607.3:c.243+12G>T | NP_001161079.1:n.243+12G>T |