HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114713823T>A , CM000663.2:g.114713823T>A | GRCh38 |
NC_000001.10:g.115256444T>A , CM000663.1:g.115256444T>A | GRCh37 |
NC_000001.9:g.115057967T>A | NCBI36 |
NG_007572.1:g.8072A>T , LRG_92:g.8072A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.267A>T MANE Select | ENSP00000358548.4:p.Ser89= | |
ENST00000369535.4:c.267A>T | ENSP00000358548.4:p.Ser89= | |
NM_002524.4:c.267A>T | NP_002515.1:p.Ser89= | |
NM_002524.5:c.267A>T MANE Select | NP_002515.1:p.Ser89= |