Linked Data
gnomAD v4:
1-63593432-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.63593432G>A , CM000663.2:g.63593432G>A | GRCh38 |
| NC_000001.10:g.64059103G>A , CM000663.1:g.64059103G>A | GRCh37 |
| NC_000001.9:g.63831691G>A | NCBI36 |
| NG_016966.1:g.5157G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371084.8:c.-57G>A (PGM1) MANE Select | ENSP00000360125.3:n.-57G>A | |
| ENST00000650546.1:c.-57G>A (PGM1) | ENSP00000497812.1:n.-57G>A | |
| ENST00000371084.7:c.-57G>A (PGM1) | ENSP00000360125.3:n.-57G>A | |
| ENST00000478138.1:n.197+93C>T (ITGB3BP) | ||
| NM_002633.2:c.-57G>A (PGM1) | NP_002624.2:n.-57G>A | |
| NM_002633.3:c.-57G>A (PGM1) MANE Select | NP_002624.2:n.-57G>A |