HGVS | Genome Assembly |
---|---|
NC_000024.10:g.20756125C>G , CM000686.2:g.20756125C>G | GRCh38 |
NC_000024.9:g.22918011C>G , CM000686.1:g.22918011C>G | GRCh37 |
NC_000024.8:g.21327399C>G | NCBI36 |
NG_032924.1:g.5058C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000629237.2:c.-39C>G MANE Select | ENSP00000486252.1:n.-39C>G | |
NM_001039567.2:c.-39C>G | NP_001034656.1:n.-39C>G | |
NM_001039567.3:c.-39C>G MANE Select | NP_001034656.1:n.-39C>G |