HGVS | Genome Assembly |
---|---|
NC_000018.10:g.13884771A= , CM000680.2:g.13884771A= | GRCh38 |
NC_000018.9:g.13884770A= , CM000680.1:g.13884770A= | GRCh37 |
NC_000018.8:g.13874770A= | NCBI36 |
NG_011819.1:g.35766T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000327606.4:c.748T= MANE Select | ENSP00000333821.2:p.Tyr250= | |
ENST00000327606.3:c.748T= | ENSP00000333821.2:p.Tyr250= | |
NM_000529.2:c.748T= MANE Select | NP_000520.1:p.Tyr250= | |
NM_001291911.1:c.748T= | NP_001278840.1:p.Tyr250= | |
XM_017025781.1:c.748T= | XP_016881270.1:p.Tyr250= |