HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18388607G= , CM000681.2:g.18388607G= | GRCh38 |
NC_000019.9:g.18499417G= , CM000681.1:g.18499417G= | GRCh37 |
NC_000019.8:g.18360417G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000595973.3:c.599G= | ENSP00000470531.3:p.Gly200= | |
ENST00000597765.2:c.599G= | ENSP00000469819.2:p.Gly200= | |
ENST00000252809.3:c.599G= MANE Select | ENSP00000252809.3:p.Gly200= | |
NM_004864.2:c.599G= | NP_004855.2:p.Gly200= | |
NM_004864.3:c.599G= | NP_004855.2:p.Gly200= | |
XM_024451789.1:c.599G= | XP_024307557.1:p.Gly200= | |
NM_004864.4:c.599G= MANE Select | NP_004855.2:p.Gly200= |