HGVS | Genome Assembly |
---|---|
NC_000010.11:g.133538803G>A , CM000672.2:g.133538803G>A | GRCh38 |
NC_000010.10:g.135352307G>A , CM000672.1:g.135352307G>A | GRCh37 |
NC_000010.9:g.135202297G>A | NCBI36 |
NG_008383.1:g.16441G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252945.8:c.1321G>A MANE Select | ENSP00000252945.3:p.Gly441Ser | |
ENST00000252945.7:c.1321G>A | ENSP00000252945.3:p.Gly441Ser | |
ENST00000368520.1:n.1358+911G>A | ||
ENST00000418356.1:c.910G>A | ENSP00000397299.1:p.Gly304Ser | |
ENST00000421586.5:c.1060G>A | ENSP00000412754.1:p.Gly354Ser | |
ENST00000463117.6:c.1321G>A | ENSP00000440689.1:p.Gly441Ser | |
ENST00000469258.1:n.417G>A | ||
ENST00000541080.5:c.737G>A | ||
NM_000773.3:c.1321G>A | NP_000764.1:p.Gly441Ser | |
NM_000773.4:c.1321G>A MANE Select | NP_000764.1:p.Gly441Ser |