HGVS | Genome Assembly |
---|---|
NC_000001.11:g.63593447A>G , CM000663.2:g.63593447A>G | GRCh38 |
NC_000001.10:g.64059118A>G , CM000663.1:g.64059118A>G | GRCh37 |
NC_000001.9:g.63831706A>G | NCBI36 |
NG_016966.1:g.5172A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371084.8:c.-42A>G (PGM1) MANE Select | ENSP00000360125.3:n.-42A>G | |
ENST00000650546.1:c.-42A>G (PGM1) | ENSP00000497812.1:n.-42A>G | |
ENST00000371084.7:c.-42A>G (PGM1) | ENSP00000360125.3:n.-42A>G | |
ENST00000478138.1:n.197+78T>C (ITGB3BP) | ||
NM_002633.2:c.-42A>G (PGM1) | NP_002624.2:n.-42A>G | |
NM_002633.3:c.-42A>G (PGM1) MANE Select | NP_002624.2:n.-42A>G |