Linked Data
gnomAD v4:
12-56041929-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.56041929G>T , CM000674.2:g.56041929G>T | GRCh38 |
| NC_000012.11:g.56435713G>T , CM000674.1:g.56435713G>T | GRCh37 |
| NC_000012.10:g.54721980G>T | NCBI36 |
| NG_023201.1:g.5028G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356464.10:c.-238G>T | ENSP00000348849.5:n.-238G>T | |
| ENST00000646449.2:c.-238G>T MANE Select | ENSP00000496643.1:n.-238G>T | |
| ENST00000356464.9:c.-238G>T | ENSP00000348849.5:n.-238G>T | |
| ENST00000552361.1:c.-170G>T | ENSP00000450339.1:n.-170G>T | |
| NM_001029.3:c.-238G>T | NP_001020.2:n.-238G>T | |
| NM_001029.5:c.-238G>T MANE Select | NP_001020.2:n.-238G>T | |
| XR_944989.3:n.75C>A | ||
| XR_944990.3:n.75C>A |