HGVS | Genome Assembly |
---|---|
NC_000005.10:g.55233374C>T , CM000667.2:g.55233374C>T | GRCh38 |
NC_000005.9:g.54529202C>T , CM000667.1:g.54529202C>T | GRCh37 |
NC_000005.8:g.54564959C>T | NCBI36 |
NG_034201.1:g.5344G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282572.5:c.150G>A MANE Select | ENSP00000282572.4:p.Pro50= | |
ENST00000282572.4:c.150G>A | ENSP00000282572.4:p.Pro50= | |
ENST00000501463.2:c.150G>A | ENSP00000422485.1:p.Pro50= | |
NM_021147.4:c.150G>A | NP_066970.3:p.Pro50= | |
NR_125346.1:n.344G>A | ||
NR_125347.1:n.344G>A | ||
NM_021147.5:c.150G>A MANE Select | NP_066970.3:p.Pro50= | |
NR_125346.2:n.235G>A | ||
NR_125347.2:n.235G>A |