HGVS | Genome Assembly |
---|---|
NC_000002.12:g.208124211G>A , CM000664.2:g.208124211G>A | GRCh38 |
NC_000002.11:g.208988935G>A , CM000664.1:g.208988935G>A | GRCh37 |
NC_000002.10:g.208697180G>A | NCBI36 |
NG_008039.1:g.5379C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264376.5:c.153C>T MANE Select | ENSP00000264376.4:p.Tyr51= | |
ENST00000264376.4:c.153C>T | ENSP00000264376.4:p.Tyr51= | |
NM_006891.3:c.153C>T | NP_008822.2:p.Tyr51= | |
NR_038437.1:n.97+4986G>A | ||
NM_006891.4:c.153C>T MANE Select | NP_008822.2:p.Tyr51= |